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Metadata
ID	DOID:0110376
Name	retinitis pigmentosa 41
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the PROM1 gene on chromosome 4p15. https://www.ncbi.nlm.nih.gov/pubmed/10587575
Xrefs	ICD10CM:H35.5 MESH:C567422 MIM:612095
Synonyms	RP41 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance