Waardenburg syndrome type 2E

Any Waardenburg syndrome type 2 in which the cause of the disease is a mutation in the SOX10 gene.

Also known as: SOX10 Waardenburg syndrome type 2, WS2E, Waardenburg syndrome type 2 caused by mutation in SOX10, Waardenburg syndrome, type 2E, Waardenburg syndrome, type 2E, with or without neurologic involvement, Ws2E, with or without neurologic involvement, hypogonadotropic hypogonadism with anosmia and deafness, with or without hypopigmentation

1 clinical trial for this condition and its sub-types, 1 tagged with Waardenburg syndrome type 2E itself.