Waardenburg syndrome type 1
MONDO:0008670Waardenburg syndrome type 1 (WS1) is a subtype of Waardenburg syndrome (WS), disorder characterized by congenital deafness, minor defects in structures arising from neural crest resulting in pigmentation anomalies of eyes, hair, and skin, in combination with dystopia canthorum.
Also known as: WS1, Waardenburg syndrome type 1, Waardenburg syndrome type I, Waardenburg syndrome with dystopia canthorum, Waardenburg syndrome, type 1, Waardenburg's syndrome type 1
5 clinical trials for this condition and its sub-types.
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Disease
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Hereditary disease
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Syndromic disease
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Human disease
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Developmental defect during embryogenesis
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Disease of genetic or genomic mechanism
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Multiple congenital anomalies/dysmorphic syndrome
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Waardenburg syndrome
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Autosomal dominant disease
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Autosomal genetic disease
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