Intellectual developmental disorder, autosomal recessive 81

Preferred Label : Intellectual developmental disorder, autosomal recessive 81;

Symbol : MRT81;

Type : Phenotype, molecular basis known;

Prefixed ID : #620700;

Details

Origin ID

620700;

UMLS CUI

C5882758;

Genes related to phenotype
- Activating signal cointegrator 1 complex, subunit 3 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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