DISEASES

Disease-gene associations mined from literature

Human genes for holoprosencephaly 9

Holoprosencephaly 9 [DOID:0110873]

A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14.

Synonyms:  holoprosencephaly 9,  DOID:0110873,  HPE9,  holoprosencephaly with microphthalmia and first branchial arch anomalies,  pituitary anomalies with holoprosencephaly-like features ...