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Waardenburg syndrome

MONDO:0018094

A disorder characterized by varying degrees of deafness and minor defects in structures arising from neural crest, including pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes.

Also known as: Waardenburg syndrome, Waardenburg's syndrome, Mende syndrome, Van der Hoeve Halbertsma Waardenburg Gualdi syndrome

5 clinical trials for this condition and its sub-types.

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Sub-types

Waardenburg syndrome type 1 (1) Waardenburg syndrome type 2 (1) Waardenburg syndrome type 2A (1) Waardenburg syndrome type 2E (1) Waardenburg-Shah syndrome (0) Waardenburg syndrome, IIa 2F (0) Waardenburg syndrome type 2B (0) Waardenburg syndrome type 2C (0) Waardenburg syndrome type 2D (0) Waardenburg syndrome type 3 (0) Waardenburg syndrome type 4A (0) Waardenburg syndrome type 4B (0) Waardenburg syndrome type 4C (0)

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) Autosomal dominant disease (0) Autosomal genetic disease (0) Disease by body system or component (0)

Trials to join now! 2 Not yet finished but already full! 1 Completed 2