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Metadata
ID	DOID:0110353
Name	retinitis pigmentosa 20
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the RPE65 gene on chromosome 1p31. https://www.ncbi.nlm.nih.gov/pubmed/9326941
Xrefs	ICD10CM:H35.5 MESH:C566718 MIM:613794
Synonyms	RP20 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance