Visualize Submit Comment

Metadata
ID	DOID:0110352
Name	retinitis pigmentosa 59
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the DHDDS gene on chromosome 1p36.11. https://www.ncbi.nlm.nih.gov/pubmed/21295283
Xrefs	ICD10CM:H35.5 OMIM:613861
Synonyms	RP59 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a autosomal recessive disease