Term Name: retinitis pigmentosa 42
Synonyms: RP42
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the KLHL7 gene on chromosome 7p15.3.
Ontology: Human Disease [DOID:0110386]   ( DOID:0110386 )

Relationships
is a type of: autosomal dominant disease retinitis pigmentosa