Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:172870 - PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY; PPCRA

Xenbase Genes: crb1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008246 - pigmented paravenous retinochoroidal atrophy

Disease Ontology (DO):
DOID:0111541 - pigmented paravenous chorioretinal atrophy