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General Information
ZIRC
OBO ID: DOID:4621
Term Name: holoprosencephaly Search Ontology:
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
  • NCI:C74988
  • OMIM:PS236100
  • ORDO:2162
  • SNOMEDCT_US_2018_03_01:30915001
  • SNOMEDCT_US_2018_03_01:44519006
  • UMLS_CUI:C0079541
Ontology: Human Disease   (DOID:4621)
OTHER holoprosencephaly PAGES
GENES INVOLVEDNo data available
PHENOTYPE No data available

CITATIONS (3)