Neurodevelopmental disorder with central hypotonia and dysmorphic facies

Preferred Label : Neurodevelopmental disorder with central hypotonia and dysmorphic facies;

Symbol : NEDCHF;

Type : Phenotype, molecular basis known;

Prefixed ID : #619797;

Details

Origin ID

619797;

UMLS CUI

C5676944;

Genes related to phenotype
- Histone deacetylase 4 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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