Term Name: retinitis pigmentosa 38
Synonyms: RP38
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the MERTK gene on chromosome 2q13.
Ontology: Human Disease [DOID:0110367]   ( DOID:0110367 )

Relationships
is a type of: autosomal recessive disease retinitis pigmentosa