|OBO ID: DOID:4621|
|Term Name:||holoprosencephaly||Search Ontology:|
|Definition:||A congenital nervous system abnormality characterized by failed or incomplete separation of the forebrain early in gestation; it is accompanied by a spectrum of characteristic craniofacial anomalies. (2)|
|Ontology:||Human Disease (DOID:4621)|
|is a type of:||
OTHER holoprosencephaly PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
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