Term Name: retinitis pigmentosa 79
Synonyms: RP79
Definition: A retinitis pigmentosa that has_material_basis_in heterozygous mutation in the HK1 gene on chromosome 10q22.
Ontology: Human Disease [DOID:0061108]   ( DOID:0061108 )

Relationships
is a type of: autosomal dominant disease retinitis pigmentosa