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DO Term : holoprosencephaly [DOID:4621] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • UMLS_CUI:C0079541,
  • GARD:6665,
  • PS236100,
  • OMIM:PS236100,
  • MESH:D016142,
  • Holoprosencephaly sequence,
  • ORDO:2162,
  • SNOMEDCT_US_2023_03_01:30915001,
  • ICD10CM:Q04.2,
  • NCI:C74988
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents