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Metadata
ID	DOID:0110388
Name	retinitis pigmentosa 10
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the IMPDH1 gene on chromosome 7q32. https://www.ncbi.nlm.nih.gov/pubmed/11875050
Xrefs	ICD10CM:H35.5 MESH:C566715 MIM:180105
Synonyms	RP10 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a autosomal dominant disease