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. [ http://purl.obolibrary.org/obo/ECO_0007646 http://purl.obolibrary.org/obo/ECO_0007638 url:http://en.wikipedia.org/wiki/Holoprosencephaly url:http://www.ncbi.nlm.nih.gov/books/NBK1530/ ]

This is just here as a test because I lose it

Term information

database cross reference
  • OMIM:PS236100
  • SNOMEDCT_US_2021_09_01:30915001
  • MESH:D016142
  • ICD10CM:Q04.2
  • GARD:6665
  • UMLS_CUI:C0079541
  • NCI:C74988
  • ORDO:2162
Subsets

DO_rare_slim, NCIthesaurus

comment
  • Xref MGI. OMIM mapping confirmed by DO. [SN].
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.
has exact synonym
  • Holoprosencephaly sequence
has obo namespace
  • disease_ontology
id
  • DOID:4621