Congenital disorder of glycosylation, type iiy

Preferred Label : Congenital disorder of glycosylation, type iiy;

Symbol : CDG2Y;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Cdg iiy; CDGIIY;

Prefixed ID : #620200;

Détails

Origin ID

620200;

UMLS CUI

C5774294;

Automatic exact mappings (from CISMeF team)
- COG5-CDG [ORDO Disease]
Genes related to phenotype
- Guided entry of tail-anchored proteins factor 4 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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