Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment

Preferred Label : Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment;

Symbol : NEDMVIC;

Type : Phenotype, molecular basis known;

Prefixed ID : #620066;

Details

Origin ID

620066;

UMLS CUI

C5774225;

Genes related to phenotype
- Deoxyhypusine hydroxylase [OMIM gene]
ORDO concept(s)
- Non-specific syndromic intellectual disability [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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