Hyperhomocysteinaemia

ICD-11 code : 3B61.00;

Preferred Label : Hyperhomocysteinaemia;

ICD-11 definition : A disease caused by deficiencies of vitamin B6, folic acid, or vitamin B12. Genetic defects in 5-MTHF reductase can consequently lead to hyperhomocysteinemia. This disease is characterised by abnormally high level of homocysteine in the blood. This disease may present with cardiovascular disease, thrombosis, schizophrenia and osteoporosis. Confirmation is by identification of deficiency in a blood sample.;

Détails

Origin ID

1993280493;

Currated CISMeF NLP mapping
- Hyperhomocysteinaemia [MedDRA Preferred Term]
- Hyperhomocysteinemia [PASCAL descriptor]
- Hyperhomocysteinemia [NCIt concept]
- Hyperhomocysteinemia [MedDRA LLT]
- Hyperhomocysteinemia (disorder) [SNOMED CT concept]
- hyperhomocysteinemia [MeSH Descriptor]
- hyperhomocysteinemia [MeSH concept]
- hyperhomocysteinemia [DO Concept]
- hyperhomocysteinemia [Disease (Nov.)]
ICD-10 Mapping
- Primary thrombophilia [ICD-10 Sub-category]

Position du mot-clé dans l'(les) arborescence(s) :

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