Terminology Service for NFDI4Health

holoprosencephaly 11

Go to external page http://purl.obolibrary.org/obo/DOID_0110877


A holoprosencephaly that has_material_basis_in heterozygous mutation in the CDON gene on chromosome 11q24. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

holoprosencephaly 11

Synonyms
  • HPE11
database cross reference
has obo namespace

disease_ontology

id

DOID:0110877