NP Core Implementation Guide
1.0.0 - Release Nepal flag

NP Core Implementation Guide - Local Development build (v1.0.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

ValueSet: ICD-11 Codes

Official URL: http://fhir.digitalhealth.gov.np/core/ValueSet/icd-11-vs Version: 1.0.0
Active as of 2026-10-14 Computable Name: ICD11VS

Value set for ICD-11 codes

References

Logical Definition (CLD)

 

Expansion

Expansion from tx.fhir.org based on codesystem ICD-11 MMS v2026-01 (CodeSystem)

This value set has >1000 codes in it. In order to keep the publication size manageable, only a selection (1000 codes) of the whole set of codes is shown

SystemCodeDisplay (en)JSONXML
http://id.who.int/icd/release/11/mms  05Endocrine, nutritional or metabolic diseases
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/461716838Endocrine diseases
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1907280211Disorders of the thyroid gland or thyroid hormones system
http://id.who.int/icd/release/11/mms  5A00Hypothyroidism
http://id.who.int/icd/release/11/mms  5A00.0Congenital hypothyroidism
http://id.who.int/icd/release/11/mms  5A00.01Permanent congenital hypothyroidism without goitre
http://id.who.int/icd/release/11/mms  5A00.00Permanent congenital hypothyroidism with diffuse goitre
http://id.who.int/icd/release/11/mms  5A00.04Congenital hypothyroidism due to iodine deficiency
http://id.who.int/icd/release/11/mms  5A00.03Transient congenital hypothyroidism
http://id.who.int/icd/release/11/mms  5A00.02Pendred syndrome
http://id.who.int/icd/release/11/mms  5A00.0YOther specified congenital hypothyroidism
http://id.who.int/icd/release/11/mms  5A00.0ZCongenital hypothyroidism, unspecified
http://id.who.int/icd/release/11/mms  5A00.1Iodine-deficiency-related thyroid disorders or allied conditions
http://id.who.int/icd/release/11/mms  5A00.11Iodine-deficiency-related multinodular goitre
http://id.who.int/icd/release/11/mms  5A00.1ZIodine-deficiency-related thyroid disorders or allied conditions, unspecified
http://id.who.int/icd/release/11/mms  5A00.10Iodine-deficiency-related diffuse goitre
http://id.who.int/icd/release/11/mms  5A00.2Acquired hypothyroidism
http://id.who.int/icd/release/11/mms  5A00.20Hypothyroidism due to medicaments or other exogenous substances
http://id.who.int/icd/release/11/mms  5A00.21Myxoedema coma
http://id.who.int/icd/release/11/mms  5A00.22Subclinical iodine-deficiency hypothyroidism
http://id.who.int/icd/release/11/mms  5A00.2YOther specified acquired hypothyroidism
http://id.who.int/icd/release/11/mms  5A00.2ZAcquired hypothyroidism, unspecified
http://id.who.int/icd/release/11/mms  5A00.ZHypothyroidism, unspecified
http://id.who.int/icd/release/11/mms  5A01Nontoxic goitre
http://id.who.int/icd/release/11/mms  5A01.0Nontoxic diffuse goitre
http://id.who.int/icd/release/11/mms  5A01.1Nontoxic single thyroid nodule
http://id.who.int/icd/release/11/mms  5A01.ZNontoxic goitre, unspecified
http://id.who.int/icd/release/11/mms  5A01.2Nontoxic multinodular goitre
http://id.who.int/icd/release/11/mms  5A02Thyrotoxicosis
http://id.who.int/icd/release/11/mms  5A02.0Thyrotoxicosis with diffuse goitre
http://id.who.int/icd/release/11/mms  5A02.1Thyrotoxicosis with toxic single thyroid nodule
http://id.who.int/icd/release/11/mms  5A02.2Thyrotoxicosis with toxic multinodular goitre
http://id.who.int/icd/release/11/mms  5A02.3Thyrotoxicosis from ectopic thyroid tissue
http://id.who.int/icd/release/11/mms  5A02.4Thyrotoxicosis factitia
http://id.who.int/icd/release/11/mms  5A02.5Thyroid crisis
http://id.who.int/icd/release/11/mms  5A02.6Secondary hyperthyroidism
http://id.who.int/icd/release/11/mms  5A02.YOther specified thyrotoxicosis
http://id.who.int/icd/release/11/mms  5A02.ZThyrotoxicosis, unspecified
http://id.who.int/icd/release/11/mms  5A03Thyroiditis
http://id.who.int/icd/release/11/mms  5A03.0Acute thyroiditis
http://id.who.int/icd/release/11/mms  5A03.1Subacute thyroiditis
http://id.who.int/icd/release/11/mms  5A03.2Autoimmune thyroiditis
http://id.who.int/icd/release/11/mms  5A03.20Hashimoto thyroiditis
http://id.who.int/icd/release/11/mms  5A03.21Painless thyroiditis
http://id.who.int/icd/release/11/mms  5A03.2YOther specified autoimmune thyroiditis
http://id.who.int/icd/release/11/mms  5A03.2ZAutoimmune thyroiditis, unspecified
http://id.who.int/icd/release/11/mms  5A03.YOther specified thyroiditis
http://id.who.int/icd/release/11/mms  5A03.ZThyroiditis, unspecified
http://id.who.int/icd/release/11/mms  5A04Hypersecretion of calcitonin
http://id.who.int/icd/release/11/mms  5A05Generalised resistance to thyroid hormone
http://id.who.int/icd/release/11/mms  5A06Sick-euthyroid syndrome
http://id.who.int/icd/release/11/mms  5A0YOther specified disorders of the thyroid gland or thyroid hormones system
http://id.who.int/icd/release/11/mms  5A0ZDisorders of the thyroid gland or thyroid hormones system, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/465177735Diabetes mellitus
http://id.who.int/icd/release/11/mms  5A10Type 1 diabetes mellitus
http://id.who.int/icd/release/11/mms  5A11Type 2 diabetes mellitus
http://id.who.int/icd/release/11/mms  5A13Diabetes mellitus, other specified type
http://id.who.int/icd/release/11/mms  5A13.0Diabetes mellitus due to genetic defects of beta cell function
http://id.who.int/icd/release/11/mms  5A13.1Diabetes mellitus due to genetic defects in insulin action
http://id.who.int/icd/release/11/mms  5A13.3Diabetes mellitus due to endocrinopathies
http://id.who.int/icd/release/11/mms  5A13.4Diabetes mellitus due to drug or chemical
http://id.who.int/icd/release/11/mms  5A13.2Diabetes mellitus due to diseases of the exocrine pancreas
http://id.who.int/icd/release/11/mms  5A13.5Diabetes mellitus due to uncommon forms of immune-mediated diabetes
http://id.who.int/icd/release/11/mms  5A13.6Diabetes mellitus due to other genetic syndromes
http://id.who.int/icd/release/11/mms  5A13.YDiabetes mellitus due to other specified cause
http://id.who.int/icd/release/11/mms  5A13.7Diabetes mellitus due to clinically defined subtypes or syndromes
http://id.who.int/icd/release/11/mms  5A12Malnutrition-related diabetes mellitus
http://id.who.int/icd/release/11/mms  5A14Diabetes mellitus, type unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1304552818Acute complications of diabetes mellitus
http://id.who.int/icd/release/11/mms  5A20Diabetic hyperosmolar hyperglycaemic state
http://id.who.int/icd/release/11/mms  5A20.0Hyperosmolar hyperglycaemic state without coma
http://id.who.int/icd/release/11/mms  5A20.1Hyperosmolar hyperglycaemic state with coma
http://id.who.int/icd/release/11/mms  5A20.ZDiabetic hyperosmolar hyperglycaemic state, unspecified
http://id.who.int/icd/release/11/mms  5A21Hypoglycaemia in the context of diabetes mellitus
http://id.who.int/icd/release/11/mms  5A21.0Hypoglycaemia in the context of diabetes mellitus without coma
http://id.who.int/icd/release/11/mms  5A21.1Hypoglycaemia in the context of diabetes mellitus with coma
http://id.who.int/icd/release/11/mms  5A21.ZHypoglycaemia in the context of diabetes, unspecified
http://id.who.int/icd/release/11/mms  5A22Diabetic acidosis
http://id.who.int/icd/release/11/mms  5A22.2Diabetic metabolic acidosis
http://id.who.int/icd/release/11/mms  5A22.0Diabetic ketoacidosis without coma
http://id.who.int/icd/release/11/mms  5A22.1Diabetic lactic acidosis
http://id.who.int/icd/release/11/mms  5A22.YOther specified diabetic acidosis
http://id.who.int/icd/release/11/mms  5A22.3Diabetic ketoacidosis with coma
http://id.who.int/icd/release/11/mms  5A22.ZDiabetic acidosis, unspecified
http://id.who.int/icd/release/11/mms  5A24Uncontrolled or unstable diabetes mellitus
http://id.who.int/icd/release/11/mms  5A23Diabetic coma
http://id.who.int/icd/release/11/mms  5A2YOther specified acute complications of diabetes mellitus
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1283179793Other disorders of glucose regulation or pancreatic internal secretion
http://id.who.int/icd/release/11/mms  5A40Intermediate hyperglycaemia
http://id.who.int/icd/release/11/mms  5A40.0Impaired fasting glucose
http://id.who.int/icd/release/11/mms  5A40.1Impaired glucose tolerance
http://id.who.int/icd/release/11/mms  5A40.YOther specified intermediate hyperglycaemia
http://id.who.int/icd/release/11/mms  5A40.ZIntermediate hyperglycaemia, unspecified
http://id.who.int/icd/release/11/mms  5A41Hypoglycaemia without associated diabetes
http://id.who.int/icd/release/11/mms  5A42Increased secretion of glucagon
http://id.who.int/icd/release/11/mms  5A43Abnormal secretion of gastrin
http://id.who.int/icd/release/11/mms  5A43.0Drug-induced hypergastrinaemia
http://id.who.int/icd/release/11/mms  5A43.YOther specified abnormal secretion of gastrin
http://id.who.int/icd/release/11/mms  5A43.1Zollinger-Ellison syndrome
http://id.who.int/icd/release/11/mms  5A43.ZAbnormal secretion of gastrin, unspecified
http://id.who.int/icd/release/11/mms  5A45Persistent hyperinsulinaemic hypoglycaemia of infancy
http://id.who.int/icd/release/11/mms  5A44Insulin-resistance syndromes
http://id.who.int/icd/release/11/mms  5A4YOther specified disorders of glucose regulation or pancreatic internal secretion
http://id.who.int/icd/release/11/mms  5A4ZDisorders of glucose regulation or pancreatic internal secretion, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/962023213Disorders of the parathyroids or parathyroid hormone system
http://id.who.int/icd/release/11/mms  5A50Hypoparathyroidism
http://id.who.int/icd/release/11/mms  5A50.0Hypoparathyroidism due to impaired parathyroid hormone secretion
http://id.who.int/icd/release/11/mms  5A50.01Secondary hypoparathyroidism
http://id.who.int/icd/release/11/mms  5A50.02Hypoparathyroidism due to destruction of the parathyroid glands
http://id.who.int/icd/release/11/mms  5A50.0YOther specified hypoparathyroidism due to impaired parathyroid hormone secretion
http://id.who.int/icd/release/11/mms  5A50.0ZHypoparathyroidism due to impaired parathyroid hormone secretion, unspecified
http://id.who.int/icd/release/11/mms  5A50.03Autoimmune hypoparathyroidism
http://id.who.int/icd/release/11/mms  5A50.00Idiopathic hypoparathyroidism
http://id.who.int/icd/release/11/mms  5A50.YOther specified hypoparathyroidism
http://id.who.int/icd/release/11/mms  5A50.1Pseudohypoparathyroidism
http://id.who.int/icd/release/11/mms  5A50.ZHypoparathyroidism, unspecified
http://id.who.int/icd/release/11/mms  5A51Hyperparathyroidism
http://id.who.int/icd/release/11/mms  5A51.0Primary hyperparathyroidism
http://id.who.int/icd/release/11/mms  5A51.1Secondary hyperparathyroidism
http://id.who.int/icd/release/11/mms  5A51.2Familial hypocalciuric hypercalcaemia
http://id.who.int/icd/release/11/mms  5A51.YOther specified hyperparathyroidism
http://id.who.int/icd/release/11/mms  5A51.ZHyperparathyroidism, unspecified
http://id.who.int/icd/release/11/mms  5A5YOther specified disorders of the parathyroids or parathyroid hormone system
http://id.who.int/icd/release/11/mms  5A5ZDisorders of the parathyroids or parathyroid hormone system, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/896961873Disorders of the pituitary hormone system
http://id.who.int/icd/release/11/mms  5A60Hyperfunction of pituitary gland
http://id.who.int/icd/release/11/mms  5A60.1Hyperprolactinaemia
http://id.who.int/icd/release/11/mms  5A60.0Acromegaly or pituitary gigantism
http://id.who.int/icd/release/11/mms  5A60.2Syndrome of inappropriate secretion of antidiuretic hormone
http://id.who.int/icd/release/11/mms  5A60.2YOther specified syndrome of inappropriate secretion of antidiuretic hormone
http://id.who.int/icd/release/11/mms  5A60.20Nephrogenic syndrome of inappropriate antidiuresis
http://id.who.int/icd/release/11/mms  5A60.2ZSyndrome of inappropriate secretion of antidiuretic hormone, unspecified
http://id.who.int/icd/release/11/mms  5A60.3Central precocious puberty
http://id.who.int/icd/release/11/mms  5A60.YOther specified hyperfunction of pituitary gland
http://id.who.int/icd/release/11/mms  5A60.ZHyperfunction of pituitary gland, unspecified
http://id.who.int/icd/release/11/mms  5A61Hypofunction or certain other specified disorders of pituitary gland
http://id.who.int/icd/release/11/mms  5A61.0Hypopituitarism
http://id.who.int/icd/release/11/mms  5A61.1Adrenocorticotropic hormone deficiency
http://id.who.int/icd/release/11/mms  5A61.2Gonadotropin deficiency
http://id.who.int/icd/release/11/mms  5A61.4Thyroid stimulating hormone deficiency
http://id.who.int/icd/release/11/mms  5A61.40Acquired central hypothyroidism
http://id.who.int/icd/release/11/mms  5A61.41Congenital central hypothyroidism
http://id.who.int/icd/release/11/mms  5A61.4YOther specified thyroid stimulating hormone deficiency
http://id.who.int/icd/release/11/mms  5A61.4ZThyroid stimulating hormone deficiency, unspecified
http://id.who.int/icd/release/11/mms  5A61.3Growth hormone deficiency
http://id.who.int/icd/release/11/mms  5A61.5Central diabetes insipidus
http://id.who.int/icd/release/11/mms  5A61.6Oxytocin deficiency
http://id.who.int/icd/release/11/mms  5A61.YOther specified hypofunction or disorders of pituitary gland
http://id.who.int/icd/release/11/mms  5A6ZDisorders of the pituitary hormone system, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/237003158Disorders of the adrenal glands or adrenal hormone system
http://id.who.int/icd/release/11/mms  5A70Cushing syndrome
http://id.who.int/icd/release/11/mms  5A70.2Pseudo-Cushing syndrome
http://id.who.int/icd/release/11/mms  5A70.0Pituitary-dependent Cushing disease
http://id.who.int/icd/release/11/mms  5A70.1Ectopic ACTH syndrome
http://id.who.int/icd/release/11/mms  5A70.3Nelson syndrome
http://id.who.int/icd/release/11/mms  5A70.YOther specified Cushing syndrome
http://id.who.int/icd/release/11/mms  5A70.ZCushing syndrome, unspecified
http://id.who.int/icd/release/11/mms  5A71Adrenogenital disorders
http://id.who.int/icd/release/11/mms  5A71.046,XX disorders of sex development induced by androgens of fetal origin
http://id.who.int/icd/release/11/mms  5A71.00Glucocorticoid resistance
http://id.who.int/icd/release/11/mms  5A71.0YOther specified 46,XX disorders of sex development induced by androgens of fetal origin
http://id.who.int/icd/release/11/mms  5A71.01Congenital adrenal hyperplasia
http://id.who.int/icd/release/11/mms  5A71.0Z46,XX disorders of sex development induced by androgens of fetal origin, unspecified
http://id.who.int/icd/release/11/mms  5A71.146,XX disorders of sex development induced by androgens of maternal origin
http://id.who.int/icd/release/11/mms  5A71.YOther specified adrenogenital disorders
http://id.who.int/icd/release/11/mms  5A71.ZAdrenogenital disorders, unspecified
http://id.who.int/icd/release/11/mms  5A72Hyperaldosteronism
http://id.who.int/icd/release/11/mms  5A72.1Secondary hyperaldosteronism
http://id.who.int/icd/release/11/mms  5A72.0Primary hyperaldosteronism
http://id.who.int/icd/release/11/mms  5A72.ZHyperaldosteronism, unspecified
http://id.who.int/icd/release/11/mms  5A73Hypoaldosteronism
http://id.who.int/icd/release/11/mms  5A74Adrenocortical insufficiency
http://id.who.int/icd/release/11/mms  5A74.0Acquired adrenocortical insufficiency
http://id.who.int/icd/release/11/mms  5A74.1Adrenal crisis
http://id.who.int/icd/release/11/mms  5A74.YOther specified adrenocortical insufficiency
http://id.who.int/icd/release/11/mms  5A74.ZAdrenocortical insufficiency, unspecified
http://id.who.int/icd/release/11/mms  5A75Adrenomedullary hyperfunction
http://id.who.int/icd/release/11/mms  5A76Certain specified disorders of adrenal gland
http://id.who.int/icd/release/11/mms  5A76.0Premature adrenarche
http://id.who.int/icd/release/11/mms  5A76.YOther specified disorders of adrenal gland
http://id.who.int/icd/release/11/mms  5A7ZDisorders of the adrenal glands or adrenal hormone system, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1465641389Disorders of the gonadal hormone system
http://id.who.int/icd/release/11/mms  5A80Ovarian dysfunction
http://id.who.int/icd/release/11/mms  5A80.1Polycystic ovary syndrome
http://id.who.int/icd/release/11/mms  5A80.0Clinical hyperandrogenism
http://id.who.int/icd/release/11/mms  5A80.2Polycystic ovary
http://id.who.int/icd/release/11/mms  5A80.3Anovulation
http://id.who.int/icd/release/11/mms  5A80.5Diminished ovarian reserve
http://id.who.int/icd/release/11/mms  5A80.4Oligo-ovulation
http://id.who.int/icd/release/11/mms  5A80.YOther specified ovarian dysfunction
http://id.who.int/icd/release/11/mms  5A80.ZOvarian dysfunction, unspecified
http://id.who.int/icd/release/11/mms  5A81Testicular dysfunction or testosterone-related disorders
http://id.who.int/icd/release/11/mms  5A81.0Testicular hyperfunction
http://id.who.int/icd/release/11/mms  5A81.1Testicular hypofunction
http://id.who.int/icd/release/11/mms  5A81.YOther specified testicular dysfunction or testosterone-related disorders
http://id.who.int/icd/release/11/mms  5A81.ZTesticular dysfunction or testosterone-related disorders, unspecified
http://id.who.int/icd/release/11/mms  5A8ZDisorders of the gonadal hormone system, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/840727139Certain disorders of puberty
http://id.who.int/icd/release/11/mms  5A92Peripheral precocious puberty
http://id.who.int/icd/release/11/mms  5A90Disorder of puberty due to oestrogen resistance
http://id.who.int/icd/release/11/mms  5A91Delayed puberty
http://id.who.int/icd/release/11/mms  5A9YOther disorders of puberty
http://id.who.int/icd/release/11/mms  5A9ZDisorders of puberty, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1465366519Polyglandular dysfunction
http://id.who.int/icd/release/11/mms  5B00Autoimmune polyendocrinopathy
http://id.who.int/icd/release/11/mms  5B0ZPolyglandular dysfunction, unspecified
http://id.who.int/icd/release/11/mms  5B0YOther specified polyglandular dysfunction
http://id.who.int/icd/release/11/mms  5B01Polyglandular hyperfunction
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/895465736Endocrine disorders, not elsewhere classified
http://id.who.int/icd/release/11/mms  5B10Carcinoid syndrome
http://id.who.int/icd/release/11/mms  5B11Short stature, not elsewhere classified
http://id.who.int/icd/release/11/mms  5B12Constitutional tall stature
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/893358872Neoplasms of the endocrine system
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1909613405Endocrine tumours
http://id.who.int/icd/release/11/mms  5B3ZEndocrine diseases, unspecified
http://id.who.int/icd/release/11/mms  5B3YOther specified endocrine diseases
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1671987290Nutritional disorders
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1517885800Undernutrition
http://id.who.int/icd/release/11/mms  5B50Underweight in infants, children or adolescents
http://id.who.int/icd/release/11/mms  5B53Stunting in infants, children or adolescents
http://id.who.int/icd/release/11/mms  5B52Acute malnutrition in infants, children or adolescents
http://id.who.int/icd/release/11/mms  5B55Vitamin A deficiency
http://id.who.int/icd/release/11/mms  5B55.0Vitamin A deficiency with night blindness
http://id.who.int/icd/release/11/mms  5B55.1Vitamin A deficiency with conjunctival xerosis
http://id.who.int/icd/release/11/mms  5B55.2Vitamin A deficiency with conjunctival xerosis and Bitot's spots
http://id.who.int/icd/release/11/mms  5B55.3Vitamin A deficiency with corneal xerosis
http://id.who.int/icd/release/11/mms  5B55.4Vitamin A deficiency with corneal ulceration or keratomalacia
http://id.who.int/icd/release/11/mms  5B55.5Vitamin A deficiency with xerophthalmic scars of cornea or blindness
http://id.who.int/icd/release/11/mms  5B55.ZVitamin A deficiency, unspecified
http://id.who.int/icd/release/11/mms  5B55.YVitamin A deficiency with other specified manifestations
http://id.who.int/icd/release/11/mms  5B54Underweight in adults
http://id.who.int/icd/release/11/mms  5B51Wasting in infants, children or adolescents
http://id.who.int/icd/release/11/mms  5B56Vitamin C deficiency
http://id.who.int/icd/release/11/mms  5B56.0Scurvy
http://id.who.int/icd/release/11/mms  5B56.YOther specified vitamin C deficiency
http://id.who.int/icd/release/11/mms  5B56.ZVitamin C deficiency, unspecified
http://id.who.int/icd/release/11/mms  5B57Vitamin D deficiency
http://id.who.int/icd/release/11/mms  5B57.0Vitamin D deficiency rickets
http://id.who.int/icd/release/11/mms  5B57.1Vitamin D deficiency osteomalacia
http://id.who.int/icd/release/11/mms  5B57.YOther specified vitamin D deficiency
http://id.who.int/icd/release/11/mms  5B57.ZVitamin D deficiency, unspecified
http://id.who.int/icd/release/11/mms  5B58Vitamin E deficiency
http://id.who.int/icd/release/11/mms  5B5AVitamin B1 deficiency
http://id.who.int/icd/release/11/mms  5B5A.0Beriberi
http://id.who.int/icd/release/11/mms  5B5A.00Dry beriberi
http://id.who.int/icd/release/11/mms  5B5A.01Wet beriberi
http://id.who.int/icd/release/11/mms  5B5A.0ZBeriberi, unspecified
http://id.who.int/icd/release/11/mms  5B5A.1Wernicke-Korsakoff Syndrome
http://id.who.int/icd/release/11/mms  5B5A.11Korsakoff syndrome
http://id.who.int/icd/release/11/mms  5B5A.10Wernicke encephalopathy
http://id.who.int/icd/release/11/mms  5B5A.1YOther specified Wernicke-Korsakoff Syndrome
http://id.who.int/icd/release/11/mms  5B5A.1ZWernicke-Korsakoff Syndrome, unspecified
http://id.who.int/icd/release/11/mms  5B5A.YOther specified vitamin B1 deficiency
http://id.who.int/icd/release/11/mms  5B5A.ZVitamin B1 deficiency, unspecified
http://id.who.int/icd/release/11/mms  5B59Vitamin K deficiency
http://id.who.int/icd/release/11/mms  5B5BVitamin B2 deficiency
http://id.who.int/icd/release/11/mms  5B5CVitamin B3 deficiency
http://id.who.int/icd/release/11/mms  5B5C.YOther specified vitamin B3 deficiency
http://id.who.int/icd/release/11/mms  5B5C.0Pellagra
http://id.who.int/icd/release/11/mms  5B5C.ZVitamin B3 deficiency, unspecified
http://id.who.int/icd/release/11/mms  5B5DVitamin B6 deficiency
http://id.who.int/icd/release/11/mms  5B5EFolate deficiency
http://id.who.int/icd/release/11/mms  5B5FVitamin B12 deficiency
http://id.who.int/icd/release/11/mms  5B5GBiotin deficiency
http://id.who.int/icd/release/11/mms  5B5JCholine deficiency
http://id.who.int/icd/release/11/mms  5B5HPantothenic acid deficiency
http://id.who.int/icd/release/11/mms  5B5KMineral deficiencies
http://id.who.int/icd/release/11/mms  5B5K.0Iron deficiency
http://id.who.int/icd/release/11/mms  5B5K.1Calcium deficiency
http://id.who.int/icd/release/11/mms  5B5K.10Tetany due to acute calcium deficiency
http://id.who.int/icd/release/11/mms  5B5K.1YOther specified calcium deficiency
http://id.who.int/icd/release/11/mms  5B5K.1ZCalcium deficiency, unspecified
http://id.who.int/icd/release/11/mms  5B5K.2Zinc deficiency
http://id.who.int/icd/release/11/mms  5B5K.3Iodine deficiency
http://id.who.int/icd/release/11/mms  5B5K.4Fluorine deficiency
http://id.who.int/icd/release/11/mms  5B5K.5Sodium chloride deficiency
http://id.who.int/icd/release/11/mms  5B5K.6Copper deficiency
http://id.who.int/icd/release/11/mms  5B5K.7Selenium deficiency
http://id.who.int/icd/release/11/mms  5B5K.8Chromium deficiency
http://id.who.int/icd/release/11/mms  5B5K.9Manganese deficiency
http://id.who.int/icd/release/11/mms  5B5K.BVanadium deficiency
http://id.who.int/icd/release/11/mms  5B5K.AMolybdenum deficiency
http://id.who.int/icd/release/11/mms  5B5K.ZMineral deficiency, unspecified
http://id.who.int/icd/release/11/mms  5B5K.YOther specified mineral deficiency
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/419506380Sequelae of malnutrition or certain specified nutritional deficiencies
http://id.who.int/icd/release/11/mms  5B60Sequelae of protein-energy malnutrition
http://id.who.int/icd/release/11/mms  5B61Sequelae of vitamin A deficiency
http://id.who.int/icd/release/11/mms  5B63Sequelae of rickets
http://id.who.int/icd/release/11/mms  5B62Sequelae of vitamin C deficiency
http://id.who.int/icd/release/11/mms  5B6YOther specified sequelae of malnutrition or certain specified nutritional deficiencies
http://id.who.int/icd/release/11/mms  5B6ZSequelae of malnutrition or certain specified nutritional deficiencies, unspecified
http://id.who.int/icd/release/11/mms  5B70Essential fatty acid deficiency
http://id.who.int/icd/release/11/mms  5B71Protein deficiency
http://id.who.int/icd/release/11/mms  5B7YOther specified undernutrition
http://id.who.int/icd/release/11/mms  5B7ZUnspecified undernutrition
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1492142148Overweight, obesity or specific nutrient excesses
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1668932342Overweight or obesity
http://id.who.int/icd/release/11/mms  5B80Overweight or localised adiposity
http://id.who.int/icd/release/11/mms  5B80.0Overweight
http://id.who.int/icd/release/11/mms  5B80.00Overweight in infants, children or adolescents
http://id.who.int/icd/release/11/mms  5B80.01Overweight in adults
http://id.who.int/icd/release/11/mms  5B80.0ZOverweight, unspecified
http://id.who.int/icd/release/11/mms  5B80.1Localised adiposity
http://id.who.int/icd/release/11/mms  5B81Obesity
http://id.who.int/icd/release/11/mms  5B81.0Obesity due to energy imbalance
http://id.who.int/icd/release/11/mms  5B81.00Obesity in children or adolescents
http://id.who.int/icd/release/11/mms  5B81.01Obesity in adults
http://id.who.int/icd/release/11/mms  5B81.1Drug-induced obesity
http://id.who.int/icd/release/11/mms  5B81.YOther specified obesity
http://id.who.int/icd/release/11/mms  5B81.ZObesity, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1840019509Certain specified nutrient excesses
http://id.who.int/icd/release/11/mms  5B90Vitamin excesses
http://id.who.int/icd/release/11/mms  5B90.0Hypervitaminosis A
http://id.who.int/icd/release/11/mms  5B90.1Hypercarotenaemia
http://id.who.int/icd/release/11/mms  5B90.3Megavitamin-B6 syndrome
http://id.who.int/icd/release/11/mms  5B90.2Hypervitaminosis D
http://id.who.int/icd/release/11/mms  5B90.YOther specified vitamin excess
http://id.who.int/icd/release/11/mms  5B90.ZUnspecified vitamin excesses
http://id.who.int/icd/release/11/mms  5B91Mineral excesses
http://id.who.int/icd/release/11/mms  5B91.2Sodium chloride excess
http://id.who.int/icd/release/11/mms  5B91.0Hypercalcaemia
http://id.who.int/icd/release/11/mms  5B91.1Zinc excess
http://id.who.int/icd/release/11/mms  5B91.3Fluorine excess
http://id.who.int/icd/release/11/mms  5B91.4Aluminium excess
http://id.who.int/icd/release/11/mms  5B91.5Manganese excess
http://id.who.int/icd/release/11/mms  5B91.YOther specified mineral excess
http://id.who.int/icd/release/11/mms  5B91.ZUnspecified mineral excess
http://id.who.int/icd/release/11/mms  5B9ZNutrient excesses, unspecified
http://id.who.int/icd/release/11/mms  5B9YOther specified nutrient excesses
http://id.who.int/icd/release/11/mms  5C1YOther specified overweight, obesity or specific nutrient excesses
http://id.who.int/icd/release/11/mms  5C3YOther specified nutritional disorders
http://id.who.int/icd/release/11/mms  5C3ZNutritional disorders, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/155258022Metabolic disorders
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/733825440Inborn errors of metabolism
http://id.who.int/icd/release/11/mms  5C50Inborn errors of amino acid or other organic acid metabolism
http://id.who.int/icd/release/11/mms  5C50.0Phenylketonuria
http://id.who.int/icd/release/11/mms  5C50.00Classical phenylketonuria
http://id.who.int/icd/release/11/mms  5C50.01Nonclassical phenylketonuria
http://id.who.int/icd/release/11/mms  5C50.02Embryofetopathy due to maternal phenylketonuria
http://id.who.int/icd/release/11/mms  5C50.0YOther specified phenylketonuria
http://id.who.int/icd/release/11/mms  5C50.0ZPhenylketonuria, unspecified
http://id.who.int/icd/release/11/mms  5C50.1Disorders of tyrosine metabolism
http://id.who.int/icd/release/11/mms  5C50.10Alkaptonuria
http://id.who.int/icd/release/11/mms  5C50.12Tyrosinaemia type 2
http://id.who.int/icd/release/11/mms  5C50.11Tyrosinaemia type 1
http://id.who.int/icd/release/11/mms  5C50.1YOther specified disorders of tyrosine metabolism
http://id.who.int/icd/release/11/mms  5C50.1ZDisorders of tyrosine metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C50.2Disorders of histidine metabolism
http://id.who.int/icd/release/11/mms  5C50.20Histidinaemia
http://id.who.int/icd/release/11/mms  5C50.21Urocanic aciduria
http://id.who.int/icd/release/11/mms  5C50.2YOther specified disorders of histidine metabolism
http://id.who.int/icd/release/11/mms  5C50.2ZDisorders of histidine metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C50.3Disorders of tryptophan metabolism
http://id.who.int/icd/release/11/mms  5C50.5Disorders of the gamma-glutamyl cycle
http://id.who.int/icd/release/11/mms  5C50.6Disorders of serine metabolism
http://id.who.int/icd/release/11/mms  5C50.7Disorders of glycine metabolism
http://id.who.int/icd/release/11/mms  5C50.70Glycine encephalopathy
http://id.who.int/icd/release/11/mms  5C50.71Sarcosinaemia
http://id.who.int/icd/release/11/mms  5C50.7ZDisorders of glycine metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C50.7YOther specified disorders of glycine metabolism
http://id.who.int/icd/release/11/mms  5C50.8Disorders of proline or hydroxyproline metabolism
http://id.who.int/icd/release/11/mms  5C50.9Disorders of ornithine metabolism
http://id.who.int/icd/release/11/mms  5C50.ADisorders of urea cycle metabolism
http://id.who.int/icd/release/11/mms  5C50.A1Carbamoylphosphate synthetase deficiency
http://id.who.int/icd/release/11/mms  5C50.A0Argininosuccinic aciduria
http://id.who.int/icd/release/11/mms  5C50.A2Argininaemia
http://id.who.int/icd/release/11/mms  5C50.AYOther specified disorders of urea cycle metabolism
http://id.who.int/icd/release/11/mms  5C50.A3Citrullinaemia
http://id.who.int/icd/release/11/mms  5C50.AZDisorders of urea cycle metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C50.BDisorders of methionine cycle or sulphur amino acid metabolism
http://id.who.int/icd/release/11/mms  5C50.CDisorders of beta or omega amino acid metabolism
http://id.who.int/icd/release/11/mms  5C50.DDisorders of branched-chain amino acid metabolism
http://id.who.int/icd/release/11/mms  5C50.D0Maple-syrup-urine disease
http://id.who.int/icd/release/11/mms  5C50.DZDisorders of branched-chain amino acid metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C50.DYOther specified disorders of branched-chain amino acid metabolism
http://id.who.int/icd/release/11/mms  5C50.EOrganic aciduria
http://id.who.int/icd/release/11/mms  5C50.E1Cerebral organic aciduria
http://id.who.int/icd/release/11/mms  5C50.E0Classical organic aciduria
http://id.who.int/icd/release/11/mms  5C50.EYOther specified organic aciduria
http://id.who.int/icd/release/11/mms  5C50.EZOrganic aciduria, unspecified
http://id.who.int/icd/release/11/mms  5C50.FDisorders of peptide metabolism
http://id.who.int/icd/release/11/mms  5C50.F1Carnosinaemia
http://id.who.int/icd/release/11/mms  5C50.F0Prolidase deficiency
http://id.who.int/icd/release/11/mms  5C50.F2Homocarnosinosis
http://id.who.int/icd/release/11/mms  5C50.FYOther specified disorders of peptide metabolism
http://id.who.int/icd/release/11/mms  5C50.FZDisorders of peptide metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C50.GTrimethylaminuria
http://id.who.int/icd/release/11/mms  5C50.YOther specified inborn errors of amino acid or other organic acid metabolism
http://id.who.int/icd/release/11/mms  5C50.ZInborn errors of amino acid or other organic acid metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C50.4Disorders of lysine or hydroxylysine metabolism
http://id.who.int/icd/release/11/mms  5C51Inborn errors of carbohydrate metabolism
http://id.who.int/icd/release/11/mms  5C51.1Disorders of glycerol metabolism
http://id.who.int/icd/release/11/mms  5C51.2Disorders of glyoxylate metabolism
http://id.who.int/icd/release/11/mms  5C51.2YOther specified disorders of glyoxylate metabolism
http://id.who.int/icd/release/11/mms  5C51.20Primary hyperoxaluria type 1
http://id.who.int/icd/release/11/mms  5C51.2ZDisorders of glyoxylate metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C51.0Disorders of the pentose phosphate pathway
http://id.who.int/icd/release/11/mms  5C51.3Glycogen storage disease
http://id.who.int/icd/release/11/mms  5C51.4Disorders of galactose metabolism
http://id.who.int/icd/release/11/mms  5C51.40Galactose-1-phosphate uridyltransferase deficiency
http://id.who.int/icd/release/11/mms  5C51.41Galactokinase deficiency
http://id.who.int/icd/release/11/mms  5C51.42Glucose or galactose intolerance of newborn
http://id.who.int/icd/release/11/mms  5C51.4YOther specified disorders of galactose metabolism
http://id.who.int/icd/release/11/mms  5C51.4ZDisorders of galactose metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C51.YOther specified inborn errors of carbohydrate metabolism
http://id.who.int/icd/release/11/mms  5C51.5Disorders of fructose metabolism
http://id.who.int/icd/release/11/mms  5C51.50Hereditary fructose intolerance
http://id.who.int/icd/release/11/mms  5C51.5YOther specified disorders of fructose metabolism
http://id.who.int/icd/release/11/mms  5C51.5ZDisorders of fructose metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C51.ZInborn errors of carbohydrate metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C52Inborn errors of lipid metabolism
http://id.who.int/icd/release/11/mms  5C52.0Inborn errors of fatty acid oxidation or ketone body metabolism
http://id.who.int/icd/release/11/mms  5C52.00Disorders of carnitine transport or the carnitine cycle
http://id.who.int/icd/release/11/mms  5C52.01Disorders of mitochondrial fatty acid oxidation
http://id.who.int/icd/release/11/mms  5C52.03Sjögren-Larsson syndrome
http://id.who.int/icd/release/11/mms  5C52.0YOther specified inborn errors of fatty acid oxidation or ketone body metabolism
http://id.who.int/icd/release/11/mms  5C52.02Disorders of ketone body metabolism
http://id.who.int/icd/release/11/mms  5C52.0ZInborn errors of fatty acid oxidation or ketone body metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C52.1Inborn errors of sterol metabolism
http://id.who.int/icd/release/11/mms  5C52.10Disorders of cholesterol synthesis
http://id.who.int/icd/release/11/mms  5C52.1YOther specified inborn errors of sterol metabolism
http://id.who.int/icd/release/11/mms  5C52.11Bile acid synthesis defect with cholestasis
http://id.who.int/icd/release/11/mms  5C52.1ZInborn errors of sterol metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C52.2Neutral lipid storage disease
http://id.who.int/icd/release/11/mms  5C52.YOther specified inborn errors of lipid metabolism
http://id.who.int/icd/release/11/mms  5C52.ZInborn errors of lipid metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C53Inborn errors of energy metabolism
http://id.who.int/icd/release/11/mms  5C53.0Disorders of pyruvate metabolism
http://id.who.int/icd/release/11/mms  5C53.00Pyruvate kinase deficiency
http://id.who.int/icd/release/11/mms  5C53.01Lactate dehydrogenase deficiency
http://id.who.int/icd/release/11/mms  5C53.02Pyruvate dehydrogenase complex deficiency
http://id.who.int/icd/release/11/mms  5C53.03Pyruvate carboxylase deficiency
http://id.who.int/icd/release/11/mms  5C53.0YOther specified disorders of pyruvate metabolism
http://id.who.int/icd/release/11/mms  5C53.0ZDisorders of pyruvate metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C53.1Disorders of the citric acid cycle
http://id.who.int/icd/release/11/mms  5C53.2Disorders of mitochondrial oxidative phosphorylation
http://id.who.int/icd/release/11/mms  5C53.21Multiple mitochondrial DNA deletion syndromes
http://id.who.int/icd/release/11/mms  5C53.23Mitochondrial protein translation defects
http://id.who.int/icd/release/11/mms  5C53.20Mitochondrial DNA depletion syndromes
http://id.who.int/icd/release/11/mms  5C53.22Coenzyme Q10 deficiency
http://id.who.int/icd/release/11/mms  5C53.24Leigh syndrome
http://id.who.int/icd/release/11/mms  5C53.25Isolated ATP synthase deficiency
http://id.who.int/icd/release/11/mms  5C53.2YOther specified disorders of mitochondrial oxidative phosphorylation
http://id.who.int/icd/release/11/mms  5C53.2ZDisorders of mitochondrial oxidative phosphorylation, unspecified
http://id.who.int/icd/release/11/mms  5C53.3Disorders of mitochondrial membrane transport
http://id.who.int/icd/release/11/mms  5C53.30Mitochondrial substrate carrier disorders
http://id.who.int/icd/release/11/mms  5C53.3ZDisorders of mitochondrial membrane transport, unspecified
http://id.who.int/icd/release/11/mms  5C53.31Mitochondrial protein import disorders
http://id.who.int/icd/release/11/mms  5C53.3YOther specified disorders of mitochondrial membrane transport
http://id.who.int/icd/release/11/mms  5C53.4Disorders of creatine metabolism
http://id.who.int/icd/release/11/mms  5C53.YOther specified inborn errors of energy metabolism
http://id.who.int/icd/release/11/mms  5C53.ZInborn errors of energy metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C54Inborn errors of glycosylation or other specified protein modification
http://id.who.int/icd/release/11/mms  5C54.1Disorders of protein O-glycosylation
http://id.who.int/icd/release/11/mms  5C54.0Disorders of protein N-glycosylation
http://id.who.int/icd/release/11/mms  5C54.2Disorders of multiple glycosylation or other pathways
http://id.who.int/icd/release/11/mms  5C54.YOther specified inborn errors of glycosylation or other specified protein modification
http://id.who.int/icd/release/11/mms  5C54.ZInborn errors of glycosylation or protein modification, unspecified
http://id.who.int/icd/release/11/mms  5C55Inborn errors of purine, pyrimidine or nucleotide metabolism
http://id.who.int/icd/release/11/mms  5C55.0Disorders of purine metabolism
http://id.who.int/icd/release/11/mms  5C55.00Xanthinuria
http://id.who.int/icd/release/11/mms  5C55.01Lesch-Nyhan syndrome
http://id.who.int/icd/release/11/mms  5C55.0ZDisorders of purine metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C55.0YOther specified disorders of purine metabolism
http://id.who.int/icd/release/11/mms  5C55.1Disorders of pyrimidine metabolism
http://id.who.int/icd/release/11/mms  5C55.2Disorders of nucleotide metabolism
http://id.who.int/icd/release/11/mms  5C55.ZInborn errors of purine, pyrimidine or nucleotide metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C55.YOther specified inborn errors of purine, pyrimidine or nucleotide metabolism
http://id.who.int/icd/release/11/mms  5C56Lysosomal diseases
http://id.who.int/icd/release/11/mms  5C56.0Sphingolipidosis
http://id.who.int/icd/release/11/mms  5C56.00Gangliosidosis
http://id.who.int/icd/release/11/mms  5C56.02Metachromatic leukodystrophy
http://id.who.int/icd/release/11/mms  5C56.01Fabry disease
http://id.who.int/icd/release/11/mms  5C56.0YOther specified sphingolipidosis
http://id.who.int/icd/release/11/mms  5C56.0ZSphingolipidosis, unspecified
http://id.who.int/icd/release/11/mms  5C56.1Neuronal ceroid lipofuscinosis
http://id.who.int/icd/release/11/mms  5C56.2Glycoproteinosis
http://id.who.int/icd/release/11/mms  5C56.20Mucolipidosis
http://id.who.int/icd/release/11/mms  5C56.21Oligosaccharidosis
http://id.who.int/icd/release/11/mms  5C56.2YOther specified glycoproteinosis
http://id.who.int/icd/release/11/mms  5C56.2ZGlycoproteinosis, unspecified
http://id.who.int/icd/release/11/mms  5C56.3Mucopolysaccharidosis
http://id.who.int/icd/release/11/mms  5C56.31Mucopolysaccharidosis type 2
http://id.who.int/icd/release/11/mms  5C56.32Mucopolysaccharidosis type 4
http://id.who.int/icd/release/11/mms  5C56.30Mucopolysaccharidosis type 1
http://id.who.int/icd/release/11/mms  5C56.33Mucopolysaccharidosis type 6
http://id.who.int/icd/release/11/mms  5C56.3YOther specified mucopolysaccharidosis
http://id.who.int/icd/release/11/mms  5C56.3ZMucopolysaccharidosis, unspecified
http://id.who.int/icd/release/11/mms  5C56.4Disorders of sialic acid metabolism
http://id.who.int/icd/release/11/mms  5C56.YOther specified lysosomal diseases
http://id.who.int/icd/release/11/mms  5C56.ZLysosomal diseases, unspecified
http://id.who.int/icd/release/11/mms  5C57Peroxisomal diseases
http://id.who.int/icd/release/11/mms  5C57.0Disorders of peroxisome biogenesis
http://id.who.int/icd/release/11/mms  5C57.1Disorders of peroxisomal alpha-, beta- or omega-oxidation
http://id.who.int/icd/release/11/mms  5C57.ZPeroxisomal diseases, unspecified
http://id.who.int/icd/release/11/mms  5C57.YOther specified peroxisomal diseases
http://id.who.int/icd/release/11/mms  5C58Inborn errors of porphyrin or heme metabolism
http://id.who.int/icd/release/11/mms  5C58.0Disorders of bilirubin metabolism or excretion
http://id.who.int/icd/release/11/mms  5C58.00Crigler-Najjar syndrome
http://id.who.int/icd/release/11/mms  5C58.01Gilbert syndrome
http://id.who.int/icd/release/11/mms  5C58.02Dubin-Johnson syndrome
http://id.who.int/icd/release/11/mms  5C58.03Progressive familial intrahepatic cholestasis
http://id.who.int/icd/release/11/mms  5C58.04Benign recurrent intrahepatic cholestasis
http://id.who.int/icd/release/11/mms  5C58.0ZDisorders of bilirubin metabolism or excretion, unspecified
http://id.who.int/icd/release/11/mms  5C58.0YOther specified disorders of bilirubin metabolism or excretion
http://id.who.int/icd/release/11/mms  5C58.1Porphyrias
http://id.who.int/icd/release/11/mms  5C58.12Erythropoietic porphyrias
http://id.who.int/icd/release/11/mms  5C58.10Porphyria cutanea tarda
http://id.who.int/icd/release/11/mms  5C58.13Variegate porphyria
http://id.who.int/icd/release/11/mms  5C58.1YOther specified porphyrias
http://id.who.int/icd/release/11/mms  5C58.1ZPorphyrias, unspecified
http://id.who.int/icd/release/11/mms  5C58.YOther specified inborn errors of porphyrin or heme metabolism
http://id.who.int/icd/release/11/mms  5C58.ZInborn errors of porphyrin or heme metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C59Inborn errors of neurotransmitter metabolism
http://id.who.int/icd/release/11/mms  5C59.0Disorders of biogenic amine metabolism
http://id.who.int/icd/release/11/mms  5C59.00Disorders of catecholamine synthesis
http://id.who.int/icd/release/11/mms  5C59.01Disorders of pterin metabolism
http://id.who.int/icd/release/11/mms  5C59.0YOther specified disorders of biogenic amine metabolism
http://id.who.int/icd/release/11/mms  5C59.0ZDisorders of biogenic amine metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C59.2Disorders of pyridoxine metabolism
http://id.who.int/icd/release/11/mms  5C59.1Disorders of gamma aminobutyric acid metabolism
http://id.who.int/icd/release/11/mms  5C59.YOther specified inborn errors of neurotransmitter metabolism
http://id.who.int/icd/release/11/mms  5C59.ZInborn errors of neurotransmitter metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C5AAlpha-1-antitrypsin deficiency
http://id.who.int/icd/release/11/mms  5C5YOther specified inborn errors of metabolism
http://id.who.int/icd/release/11/mms  5C5ZInborn errors of metabolism, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/540207810Disorders of metabolite absorption or transport
http://id.who.int/icd/release/11/mms  5C60Disorders of amino acid absorption or transport
http://id.who.int/icd/release/11/mms  5C60.1Cystinosis
http://id.who.int/icd/release/11/mms  5C60.0Oculocerebrorenal syndrome
http://id.who.int/icd/release/11/mms  5C60.2Cystinuria
http://id.who.int/icd/release/11/mms  5C60.ZDisorders of amino acid absorption or transport, unspecified
http://id.who.int/icd/release/11/mms  5C60.YOther specified disorders of amino acid absorption or transport
http://id.who.int/icd/release/11/mms  5C61Disorders of carbohydrate absorption or transport
http://id.who.int/icd/release/11/mms  5C61.2Congenital sucrase-isomaltase deficiency
http://id.who.int/icd/release/11/mms  5C61.0Glucose-galactose malabsorption
http://id.who.int/icd/release/11/mms  5C61.1Maltase-glucoamylase deficiency
http://id.who.int/icd/release/11/mms  5C61.3Alpha, alpha trehalase deficiency
http://id.who.int/icd/release/11/mms  5C61.4Acquired monosaccharide malabsorption
http://id.who.int/icd/release/11/mms  5C61.40Fructose malabsorption
http://id.who.int/icd/release/11/mms  5C61.4YOther specified acquired monosaccharide malabsorption
http://id.who.int/icd/release/11/mms  5C61.4ZAcquired monosaccharide malabsorption, unspecified
http://id.who.int/icd/release/11/mms  5C61.5Disorders of facilitated glucose transport
http://id.who.int/icd/release/11/mms  5C61.6Lactose intolerance
http://id.who.int/icd/release/11/mms  5C61.60Primary lactase deficiency
http://id.who.int/icd/release/11/mms  5C61.61Congenital lactase deficiency
http://id.who.int/icd/release/11/mms  5C61.62Secondary lactase deficiency
http://id.who.int/icd/release/11/mms  5C61.6ZLactose intolerance, unspecified
http://id.who.int/icd/release/11/mms  5C61.YOther specified disorders of carbohydrate absorption or transport
http://id.who.int/icd/release/11/mms  5C61.ZDisorders of carbohydrate absorption or transport, unspecified
http://id.who.int/icd/release/11/mms  5C62Disorders of lipid absorption or transport
http://id.who.int/icd/release/11/mms  5C63Disorders of vitamin or non-protein cofactor absorption or transport
http://id.who.int/icd/release/11/mms  5C63.0Disorders of cobalamin metabolism or transport
http://id.who.int/icd/release/11/mms  5C63.1Disorders of folate metabolism or transport
http://id.who.int/icd/release/11/mms  5C63.2Disorders of vitamin D metabolism or transport
http://id.who.int/icd/release/11/mms  5C63.20Hypocalcaemic vitamin D dependent rickets
http://id.who.int/icd/release/11/mms  5C63.21Hypocalcaemic vitamin D resistant rickets
http://id.who.int/icd/release/11/mms  5C63.22Hypophosphataemic rickets
http://id.who.int/icd/release/11/mms  5C63.2ZDisorders of vitamin D metabolism or transport, unspecified
http://id.who.int/icd/release/11/mms  5C63.2YOther specified disorders of vitamin D metabolism or transport
http://id.who.int/icd/release/11/mms  5C63.YOther specified disorders of vitamin or non-protein cofactor absorption or transport
http://id.who.int/icd/release/11/mms  5C63.ZDisorders of vitamin or non-protein cofactor absorption or transport, unspecified
http://id.who.int/icd/release/11/mms  5C64Disorders of mineral absorption or transport
http://id.who.int/icd/release/11/mms  5C64.0Disorders of copper metabolism
http://id.who.int/icd/release/11/mms  5C64.00Wilson disease
http://id.who.int/icd/release/11/mms  5C64.0YOther specified disorders of copper metabolism
http://id.who.int/icd/release/11/mms  5C64.0ZDisorders of copper metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C64.1Disorders of iron metabolism
http://id.who.int/icd/release/11/mms  5C64.10Iron overload diseases
http://id.who.int/icd/release/11/mms  5C64.1YOther specified disorders of iron metabolism
http://id.who.int/icd/release/11/mms  5C64.1ZDisorders of iron metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C64.2Disorders of zinc metabolism
http://id.who.int/icd/release/11/mms  5C64.20Acrodermatitis enteropathica
http://id.who.int/icd/release/11/mms  5C64.21Zinc deficiency syndromes
http://id.who.int/icd/release/11/mms  5C64.2ZDisorders of zinc metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C64.2YOther specified disorders of zinc metabolism
http://id.who.int/icd/release/11/mms  5C64.3Disorders of phosphorus metabolism or phosphatases
http://id.who.int/icd/release/11/mms  5C64.4Disorders of magnesium metabolism
http://id.who.int/icd/release/11/mms  5C64.40Hypermagnesaemia
http://id.who.int/icd/release/11/mms  5C64.41Hypomagnesaemia
http://id.who.int/icd/release/11/mms  5C64.4ZDisorders of magnesium metabolism, unspecified
http://id.who.int/icd/release/11/mms  5C64.5Disorders of calcium metabolism
http://id.who.int/icd/release/11/mms  5C64.6Disorders of sodium metabolism
http://id.who.int/icd/release/11/mms  5C64.7Disorders of chloride metabolism
http://id.who.int/icd/release/11/mms  5C64.YDisorders of other specified mineral absorption or transport
http://id.who.int/icd/release/11/mms  5C64.ZDisorders of mineral absorption or transport, unspecified
http://id.who.int/icd/release/11/mms  5C6ZDisorders of metabolite absorption or transport, unspecified
http://id.who.int/icd/release/11/mms  5C6YOther specified disorders of metabolite absorption or transport
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1561359275Disorders of fluid, electrolyte or acid-base balance
http://id.who.int/icd/release/11/mms  5C70Volume depletion
http://id.who.int/icd/release/11/mms  5C70.1Hypovolaemia
http://id.who.int/icd/release/11/mms  5C70.0Dehydration
http://id.who.int/icd/release/11/mms  5C70.YOther specified volume depletion
http://id.who.int/icd/release/11/mms  5C70.ZVolume depletion, unspecified
http://id.who.int/icd/release/11/mms  5C72Hypo-osmolality or hyponatraemia
http://id.who.int/icd/release/11/mms  5C71Hyperosmolality or hypernatraemia
http://id.who.int/icd/release/11/mms  5C73Acidosis
http://id.who.int/icd/release/11/mms  5C73.0Acute respiratory acidosis
http://id.who.int/icd/release/11/mms  5C73.1Chronic respiratory acidosis
http://id.who.int/icd/release/11/mms  5C73.YOther specified acidosis
http://id.who.int/icd/release/11/mms  5C73.2Anion gap metabolic acidosis
http://id.who.int/icd/release/11/mms  5C73.ZAcidosis, unspecified
http://id.who.int/icd/release/11/mms  5C75Mixed disorder of acid-base balance
http://id.who.int/icd/release/11/mms  5C74Alkalosis
http://id.who.int/icd/release/11/mms  5C76Hyperkalaemia
http://id.who.int/icd/release/11/mms  5C77Hypokalaemia
http://id.who.int/icd/release/11/mms  5C78Fluid overload
http://id.who.int/icd/release/11/mms  5C7YOther specified disorders of fluid, electrolyte or acid-base balance
http://id.who.int/icd/release/11/mms  5C7ZDisorders of fluid, electrolyte or acid-base balance, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1191191920Disorders of lipoprotein metabolism or certain specified lipidaemias
http://id.who.int/icd/release/11/mms  5C80Hyperlipoproteinaemia
http://id.who.int/icd/release/11/mms  5C80.0Hypercholesterolaemia
http://id.who.int/icd/release/11/mms  5C80.00Primary hypercholesterolaemia
http://id.who.int/icd/release/11/mms  5C80.0ZHypercholesterolaemia, unspecified
http://id.who.int/icd/release/11/mms  5C80.01Secondary hypercholesterolaemia
http://id.who.int/icd/release/11/mms  5C80.2Mixed hyperlipidaemia
http://id.who.int/icd/release/11/mms  5C80.1Hypertriglyceridaemia
http://id.who.int/icd/release/11/mms  5C80.3Hyperalphalipoproteinaemia
http://id.who.int/icd/release/11/mms  5C80.YOther specified hyperlipoproteinaemia
http://id.who.int/icd/release/11/mms  5C80.ZHyperlipoproteinaemia, unspecified
http://id.who.int/icd/release/11/mms  5C81Hypolipoproteinaemia
http://id.who.int/icd/release/11/mms  5C81.0Hypoalphalipoproteinaemia
http://id.who.int/icd/release/11/mms  5C81.YOther specified hypolipoproteinaemia
http://id.who.int/icd/release/11/mms  5C81.1Hypobetalipoproteinaemia
http://id.who.int/icd/release/11/mms  5C81.ZHypolipoproteinaemia, unspecified
http://id.who.int/icd/release/11/mms  5C8YOther specified disorders of lipoprotein metabolism or lipidaemias
http://id.who.int/icd/release/11/mms  5C8ZUnspecified disorders of lipoprotein metabolism or lipidaemias
http://id.who.int/icd/release/11/mms  5C90Metabolic or transporter liver disease
http://id.who.int/icd/release/11/mms  5C90.0Liver diseases due to urea cycle defects
http://id.who.int/icd/release/11/mms  5C90.1Liver diseases due to disorders of porphyrin or bilirubin metabolism or transport
http://id.who.int/icd/release/11/mms  5C90.3Liver disease due to disorders of lysosomal storage
http://id.who.int/icd/release/11/mms  5C90.2Liver diseases due to disorders of amino acid metabolism
http://id.who.int/icd/release/11/mms  5C90.YOther specified metabolic or transporter liver disease
http://id.who.int/icd/release/11/mms  5C90.5Liver diseases due to disorders of mineral metabolism
http://id.who.int/icd/release/11/mms  5C90.4Liver diseases due to mitochondrial disorders
http://id.who.int/icd/release/11/mms  5C90.ZMetabolic or transporter liver disease, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/393047701Other metabolic disorders
http://id.who.int/icd/release/11/mms  5D00Amyloidosis
http://id.who.int/icd/release/11/mms  5D00.0AL amyloidosis
http://id.who.int/icd/release/11/mms  5D00.1AA amyloidosis
http://id.who.int/icd/release/11/mms  5D00.2Hereditary amyloidosis
http://id.who.int/icd/release/11/mms  5D00.2YOther specified hereditary amyloidosis
http://id.who.int/icd/release/11/mms  5D00.21Non-neuropathic heredofamilial amyloidosis
http://id.who.int/icd/release/11/mms  5D00.20Hereditary ATTR amyloidosis
http://id.who.int/icd/release/11/mms  5D00.2ZHereditary amyloidosis, unspecified
http://id.who.int/icd/release/11/mms  5D00.3Dialysis-associated amyloidosis
http://id.who.int/icd/release/11/mms  5D00.YOther specified amyloidosis
http://id.who.int/icd/release/11/mms  5D00.ZAmyloidosis, unspecified
http://id.who.int/icd/release/11/mms  5D01Tumour lysis syndrome
http://id.who.int/icd/release/11/mms  5D0YOther specified metabolic disorders
http://id.who.int/icd/release/11/mms  5D2ZMetabolic disorders, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1915134721Postprocedural endocrine or metabolic disorders
http://id.who.int/icd/release/11/mms  5D40Postprocedural hypothyroidism
http://id.who.int/icd/release/11/mms  5D40.0Postirradation hypothyroidism
http://id.who.int/icd/release/11/mms  5D40.00Hypothyroidism postradioactive iodine ablation
http://id.who.int/icd/release/11/mms  5D40.0YOther specified postirradation hypothyroidism
http://id.who.int/icd/release/11/mms  5D40.0ZPostirradation hypothyroidism, unspecified
http://id.who.int/icd/release/11/mms  5D40.YOther specified postprocedural hypothyroidism
http://id.who.int/icd/release/11/mms  5D40.ZPostprocedural hypothyroidism, unspecified
http://id.who.int/icd/release/11/mms  5D41Postprocedural hypoinsulinaemia
http://id.who.int/icd/release/11/mms  5D42Postprocedural hypoparathyroidism
http://id.who.int/icd/release/11/mms  5D43Postprocedural hypopituitarism
http://id.who.int/icd/release/11/mms  5D45Postprocedural testicular hypofunction
http://id.who.int/icd/release/11/mms  5D44Postprocedural ovarian failure
http://id.who.int/icd/release/11/mms  5D46Postprocedural adrenocortical hypofunction
http://id.who.int/icd/release/11/mms  12Diseases of the respiratory system
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1971756453Upper respiratory tract disorders
http://id.who.int/icd/release/11/mms  CA00Acute nasopharyngitis
http://id.who.int/icd/release/11/mms  CA01Acute sinusitis
http://id.who.int/icd/release/11/mms  CA02Acute pharyngitis
http://id.who.int/icd/release/11/mms  CA02.0Acute bacterial pharyngitis
http://id.who.int/icd/release/11/mms  CA02.1Acute viral pharyngitis
http://id.who.int/icd/release/11/mms  CA02.1YOther specified acute viral pharyngitis
http://id.who.int/icd/release/11/mms  CA02.10Pharyngitis due to Adenovirus
http://id.who.int/icd/release/11/mms  CA02.1ZAcute viral pharyngitis, unspecified
http://id.who.int/icd/release/11/mms  CA02.YOther specified acute pharyngitis
http://id.who.int/icd/release/11/mms  CA02.ZAcute pharyngitis, unspecified
http://id.who.int/icd/release/11/mms  CA03Acute tonsillitis
http://id.who.int/icd/release/11/mms  CA03.0Streptococcal tonsillitis
http://id.who.int/icd/release/11/mms  CA03.YOther specified acute tonsillitis
http://id.who.int/icd/release/11/mms  CA03.ZAcute tonsillitis, unspecified
http://id.who.int/icd/release/11/mms  CA04Acute laryngopharyngitis
http://id.who.int/icd/release/11/mms  CA05Acute laryngitis or tracheitis
http://id.who.int/icd/release/11/mms  CA05.0Acute laryngitis
http://id.who.int/icd/release/11/mms  CA05.2Acute laryngotracheitis
http://id.who.int/icd/release/11/mms  CA05.1Acute tracheitis
http://id.who.int/icd/release/11/mms  CA06Acute obstructive laryngitis or epiglottitis
http://id.who.int/icd/release/11/mms  CA06.0Acute obstructive laryngitis
http://id.who.int/icd/release/11/mms  CA06.ZAcute obstructive laryngitis or epiglottitis, unspecified
http://id.who.int/icd/release/11/mms  CA06.1Acute epiglottitis
http://id.who.int/icd/release/11/mms  CA07Acute upper respiratory infections of multiple and unspecified sites
http://id.who.int/icd/release/11/mms  CA07.0Acute upper respiratory infection, site unspecified
http://id.who.int/icd/release/11/mms  CA07.1Acute upper respiratory infections of multiple sites
http://id.who.int/icd/release/11/mms  CA08Vasomotor or allergic rhinitis
http://id.who.int/icd/release/11/mms  CA08.0Allergic rhinitis
http://id.who.int/icd/release/11/mms  CA08.00Allergic rhinitis due to pollen
http://id.who.int/icd/release/11/mms  CA08.01Allergic rhinitis due to other seasonal allergens
http://id.who.int/icd/release/11/mms  CA08.02Allergic rhinitis due to house dust mite
http://id.who.int/icd/release/11/mms  CA08.03Other allergic rhinitis
http://id.who.int/icd/release/11/mms  CA08.0ZAllergic rhinitis, unspecified
http://id.who.int/icd/release/11/mms  CA08.1Non-allergic rhinitis
http://id.who.int/icd/release/11/mms  CA08.1YOther specified non-allergic rhinitis
http://id.who.int/icd/release/11/mms  CA08.10Non-allergic rhinitis with eosinophils
http://id.who.int/icd/release/11/mms  CA08.1ZNon-allergic rhinitis, unspecified
http://id.who.int/icd/release/11/mms  CA08.2Mixed rhinitis
http://id.who.int/icd/release/11/mms  CA08.3Vasomotor rhinitis
http://id.who.int/icd/release/11/mms  CA09Chronic rhinitis, nasopharyngitis or pharyngitis
http://id.who.int/icd/release/11/mms  CA09.0Chronic rhinitis
http://id.who.int/icd/release/11/mms  CA09.1Chronic nasopharyngitis
http://id.who.int/icd/release/11/mms  CA09.2Chronic pharyngitis
http://id.who.int/icd/release/11/mms  CA0AChronic rhinosinusitis
http://id.who.int/icd/release/11/mms  CA0A.0Samter syndrome
http://id.who.int/icd/release/11/mms  CA0A.YOther specified chronic rhinosinusitis
http://id.who.int/icd/release/11/mms  CA0A.ZChronic rhinosinusitis, unspecified
http://id.who.int/icd/release/11/mms  CA0BSilent sinus syndrome
http://id.who.int/icd/release/11/mms  CA0EHypertrophy of nasal turbinates
http://id.who.int/icd/release/11/mms  CA0DDeviated nasal septum
http://id.who.int/icd/release/11/mms  CA0CCyst or mucocele of nose or nasal sinus
http://id.who.int/icd/release/11/mms  CA0FChronic diseases of tonsils or adenoids
http://id.who.int/icd/release/11/mms  CA0F.0Hypertrophy of tonsils
http://id.who.int/icd/release/11/mms  CA0F.1Hypertrophy of adenoids
http://id.who.int/icd/release/11/mms  CA0F.3Hypertrophy of tonsils with hypertrophy of adenoids
http://id.who.int/icd/release/11/mms  CA0F.YOther specified chronic diseases of tonsils or adenoids
http://id.who.int/icd/release/11/mms  CA0F.ZChronic diseases of tonsils or adenoids, unspecified
http://id.who.int/icd/release/11/mms  CA0HDiseases of vocal cords or larynx, not elsewhere classified
http://id.who.int/icd/release/11/mms  CA0H.0Paralysis of vocal cords or larynx
http://id.who.int/icd/release/11/mms  CA0H.1Polyp of vocal cord or larynx
http://id.who.int/icd/release/11/mms  CA0H.4Laryngeal spasm
http://id.who.int/icd/release/11/mms  CA0H.3Oedema of larynx
http://id.who.int/icd/release/11/mms  CA0H.2Nodules of vocal cords
http://id.who.int/icd/release/11/mms  CA0H.YOther specified diseases of vocal cords or larynx, not elsewhere classified
http://id.who.int/icd/release/11/mms  CA0H.5Stenosis of larynx
http://id.who.int/icd/release/11/mms  CA0H.ZDiseases of vocal cords or larynx, not elsewhere classified, unspecified
http://id.who.int/icd/release/11/mms  CA0GChronic laryngitis or laryngotracheitis
http://id.who.int/icd/release/11/mms  CA0JNasal polyp
http://id.who.int/icd/release/11/mms  CA0J.0Polypoid sinus degeneration
http://id.who.int/icd/release/11/mms  CA0J.ZNasal polyp, unspecified
http://id.who.int/icd/release/11/mms  CA0J.YOther specified nasal polyp
http://id.who.int/icd/release/11/mms  CA0KAbscess of upper respiratory tract
http://id.who.int/icd/release/11/mms  CA0K.0Retropharyngeal or parapharyngeal abscess
http://id.who.int/icd/release/11/mms  CA0K.1Peritonsillar abscess
http://id.who.int/icd/release/11/mms  CA0K.ZAbscess of upper respiratory tract, unspecified
http://id.who.int/icd/release/11/mms  CA0K.YOther specified abscess of upper respiratory tract
http://id.who.int/icd/release/11/mms  CA0YOther specified upper respiratory tract disorders
http://id.who.int/icd/release/11/mms  CA0ZUpper respiratory tract disorders, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1582386590Certain lower respiratory tract diseases
http://id.who.int/icd/release/11/mms  CA20Bronchitis
http://id.who.int/icd/release/11/mms  CA20.1Chronic bronchitis
http://id.who.int/icd/release/11/mms  CA20.10Simple chronic bronchitis
http://id.who.int/icd/release/11/mms  CA20.11Mucopurulent chronic bronchitis
http://id.who.int/icd/release/11/mms  CA20.12Mixed simple and mucopurulent chronic bronchitis
http://id.who.int/icd/release/11/mms  CA20.13Protracted bacterial bronchitis
http://id.who.int/icd/release/11/mms  CA20.1YOther specified chronic bronchitis
http://id.who.int/icd/release/11/mms  CA20.1ZChronic bronchitis, unspecified
http://id.who.int/icd/release/11/mms  CA20.0Acute noninfectious bronchitis
http://id.who.int/icd/release/11/mms  CA20.YOther specified bronchitis
http://id.who.int/icd/release/11/mms  CA20.ZBronchitis, unspecified
http://id.who.int/icd/release/11/mms  CA21Emphysema
http://id.who.int/icd/release/11/mms  CA21.1Panlobular emphysema
http://id.who.int/icd/release/11/mms  CA21.0MacLeod syndrome
http://id.who.int/icd/release/11/mms  CA21.YOther specified emphysema
http://id.who.int/icd/release/11/mms  CA21.2Centrilobular emphysema
http://id.who.int/icd/release/11/mms  CA21.ZEmphysema, unspecified
http://id.who.int/icd/release/11/mms  CA22Chronic obstructive pulmonary disease
http://id.who.int/icd/release/11/mms  CA22.0Chronic obstructive pulmonary disease with acute exacerbation, unspecified
http://id.who.int/icd/release/11/mms  CA22.ZChronic obstructive pulmonary disease, unspecified
http://id.who.int/icd/release/11/mms  CA22.1Certain specified chronic obstructive pulmonary disease
http://id.who.int/icd/release/11/mms  CA23Asthma
http://id.who.int/icd/release/11/mms  CA23.0Allergic asthma
http://id.who.int/icd/release/11/mms  CA23.00Allergic asthma with exacerbation
http://id.who.int/icd/release/11/mms  CA23.01Allergic asthma with status asthmaticus
http://id.who.int/icd/release/11/mms  CA23.02Allergic asthma, uncomplicated
http://id.who.int/icd/release/11/mms  CA23.1Non-allergic asthma
http://id.who.int/icd/release/11/mms  CA23.10Non-allergic asthma with exacerbation
http://id.who.int/icd/release/11/mms  CA23.11Non-allergic asthma with status asthmaticus
http://id.who.int/icd/release/11/mms  CA23.12Non-allergic asthma, uncomplicated
http://id.who.int/icd/release/11/mms  CA23.2Other specified forms of asthma or bronchospasm
http://id.who.int/icd/release/11/mms  CA23.20Aspirin-induced asthma
http://id.who.int/icd/release/11/mms  CA23.21Exercise-induced bronchospasm
http://id.who.int/icd/release/11/mms  CA23.22Cough variant asthma
http://id.who.int/icd/release/11/mms  CA23.3Unspecified asthma
http://id.who.int/icd/release/11/mms  CA23.30Unspecified asthma with exacerbation
http://id.who.int/icd/release/11/mms  CA23.31Unspecified asthma with status asthmaticus
http://id.who.int/icd/release/11/mms  CA23.32Unspecified asthma, uncomplicated
http://id.who.int/icd/release/11/mms  CA25Cystic fibrosis
http://id.who.int/icd/release/11/mms  CA25.0Classical cystic fibrosis
http://id.who.int/icd/release/11/mms  CA25.1Atypical cystic fibrosis
http://id.who.int/icd/release/11/mms  CA25.ZCystic fibrosis, unspecified
http://id.who.int/icd/release/11/mms  CA25.2Subclinical cystic fibrosis
http://id.who.int/icd/release/11/mms  CA24Bronchiectasis
http://id.who.int/icd/release/11/mms  CA26Chronic bronchiolitis
http://id.who.int/icd/release/11/mms  CA26.0Chronic obliterative bronchiolitis
http://id.who.int/icd/release/11/mms  CA26.1Diffuse panbronchiolitis
http://id.who.int/icd/release/11/mms  CA26.YOther specified chronic bronchiolitis
http://id.who.int/icd/release/11/mms  CA26.ZChronic bronchiolitis, unspecified
http://id.who.int/icd/release/11/mms  CA27Tracheobronchitis
http://id.who.int/icd/release/11/mms  CA27.0Tracheobronchopathia osteochondroplastica
http://id.who.int/icd/release/11/mms  CA27.YOther specified tracheobronchitis
http://id.who.int/icd/release/11/mms  CA27.1Tracheobronchomegaly
http://id.who.int/icd/release/11/mms  CA27.ZTracheobronchitis, unspecified
http://id.who.int/icd/release/11/mms  CA2ZLower respiratory tract disease, unspecified
http://id.who.int/icd/release/11/mms  CA2YOther specified lower respiratory tract disease
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/915779102Lung infections
http://id.who.int/icd/release/11/mms  CA40Pneumonia
http://id.who.int/icd/release/11/mms  CA40.0Bacterial pneumonia
http://id.who.int/icd/release/11/mms  CA40.00Pneumonia due to Chlamydophila pneumoniae
http://id.who.int/icd/release/11/mms  CA40.01Pneumonia due to Escherichia coli
http://id.who.int/icd/release/11/mms  CA40.02Pneumonia due to Haemophilus influenzae
http://id.who.int/icd/release/11/mms  CA40.05Pneumonia due to Pseudomonas aeruginosa
http://id.who.int/icd/release/11/mms  CA40.03Pneumonia due to Klebsiella pneumoniae
http://id.who.int/icd/release/11/mms  CA40.06Pneumonia due to Staphylococcus
http://id.who.int/icd/release/11/mms  CA40.04Pneumonia due to Mycoplasma pneumoniae
http://id.who.int/icd/release/11/mms  CA40.08Pneumonia due to beta-haemolytic Streptococcus
http://id.who.int/icd/release/11/mms  CA40.07Pneumonia due to Streptococcus pneumoniae
http://id.who.int/icd/release/11/mms  CA40.0YPneumonia due to other specified bacteria
http://id.who.int/icd/release/11/mms  CA40.0ZBacterial pneumonia, unspecified
http://id.who.int/icd/release/11/mms  CA40.1Viral pneumonia
http://id.who.int/icd/release/11/mms  CA40.10Pneumonia due to Adenovirus
http://id.who.int/icd/release/11/mms  CA40.11Pneumonia due to Respiratory syncytial virus
http://id.who.int/icd/release/11/mms  CA40.12Pneumonia due to parainfluenza virus
http://id.who.int/icd/release/11/mms  CA40.1YPneumonia due to other specified virus
http://id.who.int/icd/release/11/mms  CA40.13Pneumonia due to Human metapneumovirus
http://id.who.int/icd/release/11/mms  CA40.1ZViral pneumonia, unspecified
http://id.who.int/icd/release/11/mms  CA40.2Fungal pneumonia
http://id.who.int/icd/release/11/mms  CA40.2YOther specified fungal pneumonia
http://id.who.int/icd/release/11/mms  CA40.20Pneumonia due to pneumocystis
http://id.who.int/icd/release/11/mms  CA40.2ZFungal pneumonia, unspecified
http://id.who.int/icd/release/11/mms  CA40.YOther specified pneumonia
http://id.who.int/icd/release/11/mms  CA40.ZPneumonia, organism unspecified
http://id.who.int/icd/release/11/mms  CA41Acute bronchiolitis
http://id.who.int/icd/release/11/mms  CA41.0Acute bronchiolitis due to respiratory syncytial virus
http://id.who.int/icd/release/11/mms  CA41.ZAcute bronchiolitis, unspecified
http://id.who.int/icd/release/11/mms  CA41.YOther specified acute bronchiolitis
http://id.who.int/icd/release/11/mms  CA42Acute bronchitis
http://id.who.int/icd/release/11/mms  CA42.0Acute bronchitis due to Streptococcus
http://id.who.int/icd/release/11/mms  CA42.1Acute bronchitis due to Rhinovirus
http://id.who.int/icd/release/11/mms  CA42.2Acute bronchitis due to Respiratory syncytial virus
http://id.who.int/icd/release/11/mms  CA42.3Acute bronchitis due to Parainfluenza virus
http://id.who.int/icd/release/11/mms  CA42.4Acute bronchitis due to Haemophilus influenzae
http://id.who.int/icd/release/11/mms  CA42.5Acute bronchitis due to Coxsackievirus
http://id.who.int/icd/release/11/mms  CA42.ZAcute bronchitis, unspecified
http://id.who.int/icd/release/11/mms  CA42.YOther specified acute bronchitis
http://id.who.int/icd/release/11/mms  CA43Abscess of lung or mediastinum
http://id.who.int/icd/release/11/mms  CA43.1Abscess of lung with pneumonia
http://id.who.int/icd/release/11/mms  CA43.0Gangrene or necrosis of lung
http://id.who.int/icd/release/11/mms  CA43.YOther specified abscess of lung or mediastinum
http://id.who.int/icd/release/11/mms  CA43.2Abscess of lung without pneumonia
http://id.who.int/icd/release/11/mms  CA43.3Abscess of mediastinum
http://id.who.int/icd/release/11/mms  CA43.ZAbscess of lung or mediastinum, unspecified
http://id.who.int/icd/release/11/mms  CA44Pyothorax
http://id.who.int/icd/release/11/mms  CA45Respiratory infections, not elsewhere classified
http://id.who.int/icd/release/11/mms  CA4YOther specified lung infections
http://id.who.int/icd/release/11/mms  CA4ZLung infections, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1332995100Lung diseases due to external agents
http://id.who.int/icd/release/11/mms  CA60Pneumoconiosis
http://id.who.int/icd/release/11/mms  CA60.0Pneumoconiosis due to dust containing silica
http://id.who.int/icd/release/11/mms  CA60.00Pneumoconiosis due to talc dust
http://id.who.int/icd/release/11/mms  CA60.0YOther specified pneumoconiosis due to dust containing silica
http://id.who.int/icd/release/11/mms  CA60.0ZPneumoconiosis due to dust containing silica, unspecified
http://id.who.int/icd/release/11/mms  CA60.1Coal worker pneumoconiosis
http://id.who.int/icd/release/11/mms  CA60.2Pneumoconiosis due to mineral fibres including asbestos
http://id.who.int/icd/release/11/mms  CA60.4Aluminosis of lung
http://id.who.int/icd/release/11/mms  CA60.3Pneumoconiosis associated with tuberculosis
http://id.who.int/icd/release/11/mms  CA60.5Bauxite fibrosis of lung
http://id.who.int/icd/release/11/mms  CA60.6Berylliosis
http://id.who.int/icd/release/11/mms  CA60.7Graphite fibrosis of lung
http://id.who.int/icd/release/11/mms  CA60.8Siderosis
http://id.who.int/icd/release/11/mms  CA60.9Stannosis
http://id.who.int/icd/release/11/mms  CA60.ZPneumoconiosis, unspecified
http://id.who.int/icd/release/11/mms  CA60.YOther specified pneumoconiosis
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/1324545867Pneumonitis
http://id.who.int/icd/release/11/mms  CA70Hypersensitivity pneumonitis due to organic dust
http://id.who.int/icd/release/11/mms  CA70.0Farmer lung
http://id.who.int/icd/release/11/mms  CA70.1Bagassosis
http://id.who.int/icd/release/11/mms  CA70.2Bird fancier lung
http://id.who.int/icd/release/11/mms  CA70.4Malt worker lung
http://id.who.int/icd/release/11/mms  CA70.3Suberosis
http://id.who.int/icd/release/11/mms  CA70.5Mushroom worker lung
http://id.who.int/icd/release/11/mms  CA70.6Maple bark stripper lung
http://id.who.int/icd/release/11/mms  CA70.7Air conditioner or humidifier lung
http://id.who.int/icd/release/11/mms  CA70.YOther specified hypersensitivity pneumonitis due to organic dust
http://id.who.int/icd/release/11/mms  CA70.ZHypersensitivity pneumonitis due to organic dust, unspecified
http://id.who.int/icd/release/11/mms  CA71Pneumonitis due to solids or liquids
http://id.who.int/icd/release/11/mms  CA71.2Pneumonitis due to aspiration of blood
http://id.who.int/icd/release/11/mms  CA71.0Pneumonitis due to inhalation of food or vomit
http://id.who.int/icd/release/11/mms  CA71.1Pneumonitis due to oils or essences
http://id.who.int/icd/release/11/mms  CA71.3Lipoid pneumonitis
http://id.who.int/icd/release/11/mms  CA71.YOther specified pneumonitis due to solids or liquids
http://id.who.int/icd/release/11/mms  CA71.ZPneumonitis due to solids or liquids, unspecified
http://id.who.int/icd/release/11/mms  CA7YOther specified pneumonitis
http://id.who.int/icd/release/11/mms  CA72Mendelson syndrome
http://id.who.int/icd/release/11/mms  CA7ZPneumonitis, unspecified
http://id.who.int/icd/release/11/mms  CA80Airway disease due to specific organic dust
http://id.who.int/icd/release/11/mms  CA80.0Byssinosis due to exposure to cotton
http://id.who.int/icd/release/11/mms  CA80.1Byssinosis due to exposure to flax
http://id.who.int/icd/release/11/mms  CA80.2Byssinosis due to exposure to cannabis
http://id.who.int/icd/release/11/mms  CA80.YOther specified airway disease due to specific organic dust
http://id.who.int/icd/release/11/mms  CA80.ZAirway disease due to specific organic dust, unspecified
http://id.who.int/icd/release/11/mms  CA81Respiratory conditions due to inhalation of chemicals, gases, fumes or vapours
http://id.who.int/icd/release/11/mms  CA81.1Pulmonary oedema due to chemicals, gases, fumes or vapours
http://id.who.int/icd/release/11/mms  CA81.0Bronchitis or pneumonitis due to chemicals, gases, fumes or vapours
http://id.who.int/icd/release/11/mms  CA81.2Upper respiratory inflammation due to chemicals, gases, fumes or vapours, not elsewhere classified
http://id.who.int/icd/release/11/mms  CA81.ZRespiratory conditions due to inhalation of chemicals, gases, fumes or vapours, unspecified
http://id.who.int/icd/release/11/mms  CA81.YOther specified respiratory conditions due to inhalation of chemicals, gases, fumes or vapours
http://id.who.int/icd/release/11/mms  CA82Respiratory conditions due to other external agents
http://id.who.int/icd/release/11/mms  CA82.0Acute pulmonary manifestations due to radiation
http://id.who.int/icd/release/11/mms  CA82.1Chronic or other pulmonary manifestations due to radiation
http://id.who.int/icd/release/11/mms  CA82.3Chronic drug-induced interstitial lung disorders
http://id.who.int/icd/release/11/mms  CA82.2Acute drug-induced interstitial lung disorders
http://id.who.int/icd/release/11/mms  CA82.4Aspergillus-induced allergic or hypersensitivity conditions
http://id.who.int/icd/release/11/mms  CA82.YOther specified respiratory conditions due to other external agents
http://id.who.int/icd/release/11/mms  CA82.ZRespiratory conditions due to other external agents, unspecified
http://id.who.int/icd/release/11/mms  CA8YOther specified lung diseases due to external agents
http://id.who.int/icd/release/11/mms  CA8ZLung diseases due to external agents, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/111658096Respiratory diseases principally affecting the lung interstitium
http://id.who.int/icd/release/11/mms  CB01Pulmonary oedema
http://id.who.int/icd/release/11/mms  CB00Acute respiratory distress syndrome
http://id.who.int/icd/release/11/mms  CB02Pulmonary eosinophilia
http://id.who.int/icd/release/11/mms  CB02.1Idiopathic eosinophilic pneumonitis
http://id.who.int/icd/release/11/mms  CB02.1YOther specified idiopathic eosinophilic pneumonitis
http://id.who.int/icd/release/11/mms  CB02.1ZIdiopathic eosinophilic pneumonitis, unspecified
http://id.who.int/icd/release/11/mms  CB02.11Idiopathic chronic eosinophilic pneumonitis
http://id.who.int/icd/release/11/mms  CB02.10Idiopathic acute eosinophilic pneumonitis
http://id.who.int/icd/release/11/mms  CB02.0Asthmatic pulmonary eosinophilia
http://id.who.int/icd/release/11/mms  CB02.2Tropical pulmonary eosinophilia
http://id.who.int/icd/release/11/mms  CB02.YOther specified pulmonary eosinophilia
http://id.who.int/icd/release/11/mms  CB02.ZPulmonary eosinophilia, unspecified
http://id.who.int/icd/release/11/mms  CB03Idiopathic interstitial pneumonitis
http://id.who.int/icd/release/11/mms  CB03.0Acute interstitial pneumonitis
http://id.who.int/icd/release/11/mms  CB03.1Combined pulmonary fibrosis and emphysema syndrome
http://id.who.int/icd/release/11/mms  CB03.2Cryptogenic organizing pneumonitis
http://id.who.int/icd/release/11/mms  CB03.4Idiopathic pulmonary fibrosis
http://id.who.int/icd/release/11/mms  CB03.3Desquamative interstitial pneumonitis
http://id.who.int/icd/release/11/mms  CB03.ZIdiopathic interstitial pneumonitis, unspecified
http://id.who.int/icd/release/11/mms  CB03.5Lymphoid interstitial pneumonia
http://id.who.int/icd/release/11/mms  CB03.YOther specified idiopathic interstitial pneumonitis
http://id.who.int/icd/release/11/mms  CB03.6Respiratory bronchiolitis - interstitial lung disease
http://id.who.int/icd/release/11/mms  CB04Primary interstitial lung diseases specific to infancy or childhood
http://id.who.int/icd/release/11/mms  CB04.0Diffuse pulmonary developmental disorders
http://id.who.int/icd/release/11/mms  CB04.1Pulmonary lymphatic dysplasia syndromes
http://id.who.int/icd/release/11/mms  CB04.2Disorders of surfactant metabolism
http://id.who.int/icd/release/11/mms  CB04.3Alveolar or peri-alveolar conditions
http://id.who.int/icd/release/11/mms  CB04.30Idiopathic pulmonary haemosiderosis
http://id.who.int/icd/release/11/mms  CB04.31Pulmonary alveolar proteinosis
http://id.who.int/icd/release/11/mms  CB04.3YOther specified alveolar or peri-alveolar conditions
http://id.who.int/icd/release/11/mms  CB04.3ZAlveolar or peri-alveolar conditions, unspecified
http://id.who.int/icd/release/11/mms  CB04.4Pulmonary capillaritis
http://id.who.int/icd/release/11/mms  CB04.6Chronic pneumonitis of infancy
http://id.who.int/icd/release/11/mms  CB04.YOther specified primary interstitial lung diseases specific to infancy or childhood
http://id.who.int/icd/release/11/mms  CB04.5Brain-lung-thyroid syndrome
http://id.who.int/icd/release/11/mms  CB04.ZPrimary interstitial lung diseases specific to infancy or childhood, unspecified
http://id.who.int/icd/release/11/mms  CB04.7Neuroendocrine cell hyperplasia of infancy
http://id.who.int/icd/release/11/mms  CB05Interstitial lung diseases associated with systemic diseases
http://id.who.int/icd/release/11/mms  CB05.0Diffuse alveolar damage
http://id.who.int/icd/release/11/mms  CB05.2Interstitial lung diseases associated with granulomatous diseases
http://id.who.int/icd/release/11/mms  CB05.1Interstitial lung diseases associated with connective tissue diseases
http://id.who.int/icd/release/11/mms  CB05.3Interstitial lung diseases associated with metabolic diseases
http://id.who.int/icd/release/11/mms  CB05.4Interstitial lung diseases associated with systemic vasculitides
http://id.who.int/icd/release/11/mms  CB05.40Respiratory disorders in Churg-Strauss syndrome
http://id.who.int/icd/release/11/mms  CB05.41Respiratory disorders in microscopic polyangiitis
http://id.who.int/icd/release/11/mms  CB05.4YOther specified interstitial lung diseases associated with systemic vasculitides
http://id.who.int/icd/release/11/mms  CB05.4ZInterstitial lung diseases associated with systemic vasculitides, unspecified
http://id.who.int/icd/release/11/mms  CB05.5Secondary pulmonary haemosiderosis
http://id.who.int/icd/release/11/mms  CB05.YOther specified interstitial lung diseases associated with systemic diseases
http://id.who.int/icd/release/11/mms  CB05.ZInterstitial lung diseases associated with systemic diseases, unspecified
http://id.who.int/icd/release/11/mms  CB06Pulmonary alveolar microlithiasis
http://id.who.int/icd/release/11/mms  CB07Lymphangioleiomyomatosis
http://id.who.int/icd/release/11/mms  CB07.0Lymphangioleiomyomatosis associated with tuberous sclerosis complex
http://id.who.int/icd/release/11/mms  CB07.YOther specified lymphangioleiomyomatosis
http://id.who.int/icd/release/11/mms  CB07.1Sporadic lymphangioleiomyomatosis
http://id.who.int/icd/release/11/mms  CB07.ZLymphangioleiomyomatosis, unspecified
http://id.who.int/icd/release/11/mms  CB0YOther specified respiratory diseases principally affecting the lung interstitium
http://id.who.int/icd/release/11/mms  CB0ZRespiratory diseases principally affecting the lung interstitium, unspecified
http://id.who.int/icd/release/11/mms  http://id.who.int/icd/release/11/mms/390439470Pleural, diaphragm or mediastinal disorders
http://id.who.int/icd/release/11/mms  CB21Pneumothorax
http://id.who.int/icd/release/11/mms  CB21.0Spontaneous tension pneumothorax
http://id.who.int/icd/release/11/mms  CB21.1Other spontaneous pneumothorax
http://id.who.int/icd/release/11/mms  CB21.YOther specified pneumothorax
http://id.who.int/icd/release/11/mms  CB21.ZPneumothorax, unspecified
http://id.who.int/icd/release/11/mms  CB20Pleural plaque
http://id.who.int/icd/release/11/mms  CB22Diseases of mediastinum, not elsewhere classified
http://id.who.int/icd/release/11/mms  CB22.0Fibrosing mediastinitis
http://id.who.int/icd/release/11/mms  CB22.ZDisease of mediastinum, unspecified
http://id.who.int/icd/release/11/mms  CB22.YOther specified diseases of mediastinum, not elsewhere classified
http://id.who.int/icd/release/11/mms  CB23Disorders of diaphragm
http://id.who.int/icd/release/11/mms  CB24Chylous effusion
http://id.who.int/icd/release/11/mms  CB25Fibrothorax
http://id.who.int/icd/release/11/mms  CB26Haemothorax
http://id.who.int/icd/release/11/mms  CB27Pleural effusion
http://id.who.int/icd/release/11/mms  CB2YOther specified pleural, diaphragm or mediastinal disorders
http://id.who.int/icd/release/11/mms  CB2ZPleural, diaphragm or mediastinal disorders, unspecified
http://id.who.int/icd/release/11/mms  CB40Certain diseases of the respiratory system
http://id.who.int/icd/release/11/mms  CB40.0Ciliary dyskinesia
http://id.who.int/icd/release/11/mms  CB40.2Pulmonary collapse
http://id.who.int/icd/release/11/mms  CB40.1Young syndrome
http://id.who.int/icd/release/11/mms  CB40.3Interstitial emphysema
http://id.who.int/icd/release/11/mms  CB40.4Compensatory emphysema
http://id.who.int/icd/release/11/mms  CB40.YOther specified diseases of the respiratory system
http://id.who.int/icd/release/11/mms  CB41Respiratory failure
http://id.who.int/icd/release/11/mms  CB41.0Acute respiratory failure

Description of the above table(s).