Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures

Preferred Label : Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures;

Symbol : NEDMIMS;

Type : Phenotype, molecular basis known;

Prefixed ID : #620023;

Details

Origin ID

620023;

UMLS CUI

C5774208;

Genes related to phenotype
- Choline kinase, alpha [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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