Adams-Oliver Syndrome

About the Disease
Adams-Oliver Syndrome, also known as congenital scalp defects with distal limb reduction anomalies, is related to adams-oliver syndrome 2 and adams-oliver syndrome 1, and has symptoms including seizures An important gene associated with Adams-Oliver Syndrome is NOTCH1 (Notch Receptor 1), and among its related pathways/superpathways are Signal Transduction and Disease. Affiliated tissues include skin, bone and eye, and related phenotypes are failure to thrive and absent toe

Common Targets
G4851 | DOCK6 | PNPLA6 | ARHGAP31 | DLL4 | EOGT | RBPJ

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