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Entry | Name | Description | Category | Pathway | Gene |
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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] |
[ KEGG | DISEASE | DRUG | MEDICUS ] |