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