Neurodevelopmental disorder with neuromuscular and skeletal abnormalities

Preferred Label : Neurodevelopmental disorder with neuromuscular and skeletal abnormalities;

Symbol : NEDNMS;

Type : Phenotype, molecular basis known;

Prefixed ID : #619833;

Details

Origin ID

619833;

UMLS CUI

C5676965;

Genes related to phenotype
- Neuronal cell adhesion molecule [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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