Visualize Submit Comment
Metadata
ID DOID:0110371
Name retinitis pigmentosa 56
Definition A retinitis pigmentosa that has_material_basis_in mutation in the IMPG2 gene on chromosome 3q12.3.
https://www.ncbi.nlm.nih.gov/pubmed/20673862
Xrefs

ICD10CM:H35.5

MIM:613581

Synonyms

RP56 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal recessive disease

Add an item to the term tracker