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Summary Literature (1)
MIM:124500 - VOHWINKEL SYNDROME; VOWNKL

Xenbase Genes: gjb2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007422 - keratoderma hereditarium mutilans

Disease Ontology (DO):
DOID:0111339 - Vohwinkel syndrome