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Entry Name Description Category Pathway Gene
H02633 Beck-Fahrner syndrome ... growth abnormalities, and characteristic craniofacial features. It has been reported that mutations in TET3 cause this disease. TET3 is a methylcytosine dioxygenase that initiates DNA demethylation during ... Congenital malformation TET3 [HSA:200424] [KO:K24309]
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