familial methionine malabsorption

Preferred Label : familial methionine malabsorption;

Origin ID

D6-B4320;

UMLS CUI

C0268622;

Currated CISMeF NLP mapping
- Familial methionine malabsorption (disorder) [SNOMED CT concept]
- Methionine malabsorption syndrome [OMIM Phenotype]
- methionine malabsorption syndrome [MeSH concept]
- methionine malabsorption syndrome [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Disorders of sulfur-bearing amino-acid metabolism [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Familial methionine malabsorption (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial methionine malabsorption (disorder) [SNOMED CT concept]
- Methionine malabsorption syndrome [OMIM Phenotype]
- methionine malabsorption syndrome [MeSH Supplementary Concept]
- methionine malabsorption syndrome [MeSH concept]