Neurodevelopmental disorder with microcephaly, short stature, and speech delay

Preferred Label : Neurodevelopmental disorder with microcephaly, short stature, and speech delay;

Symbol : NEDMISS;

Type : Phenotype, molecular basis known;

Prefixed ID : #620027;

Details

Origin ID

620027;

UMLS CUI

C5774211;

Genes related to phenotype
- Trafficking protein particle complex, subunit 10 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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