Lipodystrophy, familial partial, type 9

Preferred Label : Lipodystrophy, familial partial, type 9;

Symbol : FPLD9;

Type : Phenotype, molecular basis known;

Prefixed ID : #620683;

Details

Origin ID

620683;

UMLS CUI

C5882746;

Genes related to phenotype
- Phospholipase a and acyltransferase 3 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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