Term Name:	holoprosencephaly 9
Synonyms:	holoprosencephaly with microphthalmia and first branchial arch anomalies, HPE9, pituitary anomalies with holoprosencephaly-like features
Definition:	A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14.
Ontology:	Human Disease [DOID:0110873]   ( DOID:0110873 )