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