Terminology Service for NFDI4Health

holoprosencephaly 4

Go to external page http://purl.obolibrary.org/obo/DOID_0110880


A holoprosencephaly that has_material_basis_in heterozygous mutation in the TGIF gene on chromosome 18p11. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

holoprosencephaly 4

Synonyms
  • HPE4
database cross reference
has obo namespace

disease_ontology

id

DOID:0110880