inherited methylmalonic acidemia and homocystinuria

Preferred Label : inherited methylmalonic acidemia and homocystinuria;

Origin ID

D6-B1580;

UMLS CUI

C0268591;

Currated CISMeF NLP mapping
- Inherited methylmalonic acidemia AND homocystinuria (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Other disorders of branched-chain amino-acid metabolism [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Inherited methylmalonic acidemia AND homocystinuria (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Adenosylcobalamin and methylcobalamin synthesis defect (disorder) [SNOMED CT concept]
- Inherited methylmalonic acidemia AND homocystinuria (disorder) [SNOMED CT concept]