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Metadata
ID	DOID:0110383
Name	retinitis pigmentosa 7
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/1749427
Xrefs	ICD10CM:H35.5 MESH:C564284 OMIM:608133
Synonyms	RP7 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a digenic disease is_a autosomal recessive disease is_a autosomal dominant disease