Term Name: retinitis pigmentosa 37
Synonyms: RP37
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the NR2E3 gene on chromosome 15q23.
Ontology: Human Disease [DOID:0110399]   ( DOID:0110399 )

Relationships
is a type of: autosomal dominant disease autosomal recessive disease retinitis pigmentosa