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Metadata
ID	DOID:0110367
Name	retinitis pigmentosa 38
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the MERTK gene on chromosome 2q13. https://www.ncbi.nlm.nih.gov/pubmed/11062461
Xrefs	ICD10CM:H35.5 MIM:613862
Synonyms	RP38 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance