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Metadata
ID	DOID:0110403
Name	retinitis pigmentosa 13
Definition	A retinitis pigmentosa that has_material_basis_in mutations in the PRPF8 gene on chromosome 17p13.3. https://www.ncbi.nlm.nih.gov/pubmed/11468273
Xrefs	ICD10CM:H35.5 MESH:C564008 OMIM:600059
Synonyms	RP13 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a autosomal dominant disease