SIL HIE Implementation Guide
0.1.0 - sil-hie-active

SIL HIE Implementation Guide, published by Kathurima Kimathi. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/savannahghi/hie-fhir-ig-profile/ and changes regularly. See the Directory of published versions

ValueSet: All ICD-11 codes

Official URL: https://nshr.dha.go.ke/fhir/ValueSet/ICD11Codes Version: 0.1.0
Active as of 2026-09-05 Computable Name: ICD11Codes

All codes from ICD-11

References

This value set is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)

Logical Definition (CLD)

  • Include all codes defined in http://id.who.int/icd/release/11/mms version Not Stated (use latest from terminology server)

 

Expansion

Expansion from tx.fhir.org based on codesystem mms version 2026-01

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

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code