DISEASES

Disease-gene associations mined from literature

Human genes for cone-rod dystrophy 12

Cone-rod dystrophy 12 [DOID:0111019]

A cone-rod dystrophy that has_material_basis_in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15.

Synonyms:  cone-rod dystrophy 12,  conerod dystrophy 12,  DOID:0111019,  CORD12