Neurodevelopmental disorder with language delay and variable cognitive abnormalities

Preferred Label : Neurodevelopmental disorder with language delay and variable cognitive abnormalities;

Symbol : NEDLC;

Type : Phenotype, molecular basis known;

Prefixed ID : #620502;

Details

Origin ID

620502;

UMLS CUI

C5882689;

Genes related to phenotype
- Gamma-aminobutyric acid b receptor 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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