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
  • GARD:6665
  • ICD10CM:Q04.2
  • MESH:D016142
  • MIM:PS236100
  • NCI:C74988
  • ORDO:2162
  • SNOMEDCT_US_2023_03_01:30915001
  • UMLS_CUI:C0079541
Ontology
Human Disease   ( DOID:4621 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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