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Metadata
ID	DOID:0110399
Name	retinitis pigmentosa 37
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the NR2E3 gene on chromosome 15q23. https://www.ncbi.nlm.nih.gov/pubmed/17564971
Xrefs	ICD10CM:H35.5 MESH:C567005 MIM:611131
Synonyms	RP37 [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a retinitis pigmentosa is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance has material basis in some autosomal recessive inheritance