Phenotype

Retinal dystrophy

HPO: HP:0000556 | MedGen: search

Overview

Term
retinal dystrophy
HPO
HP:0000556
OMIM
-
In SaudiVarKB
121 articles, 121 mentions

Synonyms

None recorded

External resources

121Publications74Co-reported genes70Variants in these articles2Saudi regionsOpenLiterature network

Co-reported genes

Genes named in the same articles as retinal dystrophy. Co-mention, not a proven association.

and 49 more

Variants in these articles

Variants reported in articles that mention retinal dystrophy; the gene is shown only when the link was confirmed by dbSNP or LitVar2.

and 45 more

Saudi regions

RegionArticles
Riyadh2
Eastern Province1