DISEASES

Disease-gene associations mined from literature

Human genes for achromatopsia 4

Achromatopsia 4 [DOID:0110010]

An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the GNAT2 gene on chromosome 1p13.

Synonyms:  achromatopsia 4,  DOID:0110010,  ACHM4