Alpha-Methylacyl-CoA racemase deficiency

Preferred Label : Alpha-Methylacyl-CoA racemase deficiency;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566068;

UMLS CUI

C3280428;

Automatic exact mappings (from CISMeF team)
- Congenital bile acid synthesis defect type 4 [ICD-11 More detail]
- Congenital bile acid synthesis defect type 4 [ORDO Disease]
Currated CISMeF NLP mapping
- Alpha-Methylacyl-CoA Racemase Deficiency [NCIt concept]
- Alpha-methylacyl-CoA racemase deficiency disorder (disorder) [SNOMED CT concept]
- Alpha-methylacyl-coa racemase deficiency [OMIM Phenotype]
- alpha-methylacyl-CoA racemase deficiency [DO Concept]
Related record
- Alpha-Methylacyl-CoA racemase deficiency [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alpha-Methylacyl-CoA Racemase Deficiency [NCIt concept]
- Alpha-methylacyl-CoA racemase deficiency disorder (disorder) [SNOMED CT concept]
- Alpha-methylacyl-coa racemase deficiency [OMIM Phenotype]
- alpha-methylacyl-CoA racemase deficiency [DO Concept]