Terminology Service for NFDI4Health

holoprosencephaly

Go to external page http://purl.obolibrary.org/obo/DOID_4621


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 ]

Term info

Label

holoprosencephaly

Synonyms
  • Holoprosencephaly sequence
database cross reference
Subsets

DO_rare_slim, NCIthesaurus

comment

Xref MGI. OMIM mapping confirmed by DO. [SN].

has obo namespace

disease_ontology

id

DOID:4621