Term Name: retinitis pigmentosa 89
Synonyms: RP89
Definition: A retinitis pigmentosa characterized by onset of retinitis pigmentosa in the first decade of life and additional features of ciliopathy that has_material_basis_in heterozygous mutation in the KIF3B gene on chromosome 20q11.21.
Ontology: Human Disease [DOID:0112146]   ( DOID:0112146 )

Relationships
is a type of: autosomal dominant disease retinitis pigmentosa