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Metadata
ID	DOID:0110366
Name	retinitis pigmentosa 33
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the SNRNP200 gene on chromosome 2q11. https://www.ncbi.nlm.nih.gov/pubmed/19878916
Xrefs	ICD10CM:H35.5 MESH:C563676 MIM:610359
Synonyms	RP33 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a autosomal dominant disease