Terminology Service for NFDI4Health

holoprosencephaly 5

Go to external page http://purl.obolibrary.org/obo/DOID_0110878


A holoprosencephaly that has_material_basis_in heterozygous mutation in the ZIC2 gene on chromosome 13q32. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

holoprosencephaly 5

Synonyms
  • HPE5
database cross reference
has obo namespace

disease_ontology

id

DOID:0110878