Waardenburg syndrome type 2
MONDO:0019517Waardenburg syndrome type 2 (WS2) is an autosomal dominant subtype of Waardenburg syndrome (WS), characterized by varying degrees of deafness and pigmentation anomalies of eyes, hair and skin, but without dystopia canthorum.
Also known as: WS2, Waardenburg syndrome type 2, Waardenburg syndrome type II, WS 2, WS type 2
5 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
Disease
(618)
Hereditary disease
(172)
Syndromic disease
(24)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Disease of genetic or genomic mechanism
(2)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Waardenburg syndrome
(1)
Autosomal dominant disease
(0)
Autosomal genetic disease
(0)