Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities

Preferred Label : Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities;

Symbol : NEDGFC;

Type : Phenotype, molecular basis known;

Prefixed ID : #620113;

Details

Origin ID

620113;

UMLS CUI

C5774251;

Genes related to phenotype
- Fra10a-associated cgg repeat 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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