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Metadata
ID	DOID:0110386
Name	retinitis pigmentosa 42
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the KLHL7 gene on chromosome 7p15.3. https://www.ncbi.nlm.nih.gov/pubmed/19520207
Xrefs	ICD10CM:H35.5 MESH:C567854 OMIM:612943
Synonyms	RP42 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a autosomal dominant disease