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Metadata
ID	DOID:0110357
Name	retinitis pigmentosa 35
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the SEMA4A gene on chromosome 1q22. https://www.ncbi.nlm.nih.gov/pubmed/16199541
Xrefs	ICD10CM:H35.5 MESH:C565206 MIM:610282
Synonyms	RP35 [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