Visualize Submit Comment

Metadata
ID	DOID:0110358
Name	retinitis pigmentosa 12
Definition	A retinitis pigmentosa that has_material_basis_in mutation in the CRB1 gene on chromosome 1q31.3. https://www.ncbi.nlm.nih.gov/pubmed/10508521
Xrefs	ICD10CM:H35.5 MESH:C563999 OMIM:600105
Synonyms	RP12 [EXACT]
Parent Relationships	is_a retinitis pigmentosa is_a autosomal recessive disease