Terminology Service for NFDI4Health

holoprosencephaly 3

Go to external page http://purl.obolibrary.org/obo/DOID_0110875


A holoprosencephaly that has_material_basis_in heterozygous mutation in the SHH gene on chromosome 7q36. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

holoprosencephaly 3

Synonyms
  • HLP3
  • HPE3
database cross reference
has obo namespace

disease_ontology

id

DOID:0110875