Visualize Submit Comment
Metadata
ID DOID:0110377
Name retinitis pigmentosa 49
Definition A retinitis pigmentosa that has_material_basis_in mutation in the CNGA1 gene on chromosome 4p12.
https://www.ncbi.nlm.nih.gov/pubmed/7479749
Xrefs

ICD10CM:H35.5

OMIM:613756

Synonyms

RP49 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

Add an item to the term tracker