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Summary Literature (1)
MIM:217700 - CORNEAL ENDOTHELIAL DYSTROPHY; CHED

Xenbase Genes: slc4a11

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009019 - congenital hereditary endothelial dystrophy of cornea

Disease Ontology (DO):
DOID:0060649 - congenital hereditary endothelial dystrophy of cornea