Lipodystrophy, congenital generalized, type 5

Preferred Label : Lipodystrophy, congenital generalized, type 5;

Symbol : CGL5;

Type : Phenotype, molecular basis known;

Prefixed ID : #620680;

Details

Origin ID

620680;

UMLS CUI

C5882745;

Genes related to phenotype
- Phosphate cytidylyltransferase 1, choline, alpha isoform [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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