Waardenburg syndrome type 2C

MONDO:0011697

A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has material basis in variation in the chromosome region 8p23.

Also known as: WS2C, Waardenburg syndrome, type 2C

0 clinical trials for this condition and its sub-types, 0 tagged with Waardenburg syndrome type 2C itself.

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Including sub-types (0) Tagged with Waardenburg syndrome type 2C (0)

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