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Summary Literature (4)
MIM:148210 - KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT; KIDAD

Xenbase Genes: gjb2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007850 - autosomal dominant keratitis-ichthyosis-hearing loss syndrome

Disease Ontology (DO):
DOID:0060871 - autosomal dominant keratitis-ichthyosis-deafness syndrome