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Summary Literature (0)
MIM:172870 - PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY; PPCRA

Xenbase Genes: crb1

Human Disease Resource: OMIM

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

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