Term Name: retinitis pigmentosa 92
Synonyms: RP92
Definition: A retinitis pigmentosa characterized by relatively mild disease, with onset of night blindness and vision loss in the third to sixth decades of life that has_material_basis_in homozygous mutation in the HKDC1 gene on chromosome 10q22.
Ontology: Human Disease [DOID:0061107]   ( DOID:0061107 )

Relationships
is a type of: autosomal recessive disease retinitis pigmentosa