Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects

Preferred Label : Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects;

Symbol : NEDCDS;

Type : Phenotype, molecular basis known;

Prefixed ID : #620083;

Details

Origin ID

620083;

UMLS CUI

C5774235;

Genes related to phenotype
- Heterogeneous nuclear ribonucleoprotein h1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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