Neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities

Preferred Label : Neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities;

Symbol : NEDFBA;

Type : Phenotype, molecular basis known;

Prefixed ID : #620489;

Details

Origin ID

620489;

UMLS CUI

C5882684;

Genes related to phenotype
- Splicing factor, serine/arginine-rich, 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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