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Summary Literature (0)
MIM:108985 - SVEINSSON CHORIORETINAL ATROPHY; SCRA

Xenbase Genes: tead1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007176 - helicoid peripapillary chorioretinal degeneration

Disease Ontology (DO):
DOID:0111228 - Sveinsson chorioretinal atrophy