Search Ontology:
Human Disease

holoprosencephaly

Term ID
DOID:4621
Synonyms
  • Holoprosencephaly sequence
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)
References
Ontology
Human Disease   ( DOID:4621 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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