Acces syndrome

Preferred Label : Acces syndrome;

Symbol : ACCES;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Aplasia cutis congenita with ectrodactyly skeletal syndrome;

Prefixed ID : #619959;

Details

Origin ID

619959;

UMLS CUI

C5677019;

Genes related to phenotype
- Ubiquitin-like modifier-activating enzyme 2 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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