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Waardenburg syndrome

rare

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.

Identifiers
MONDO:0018094 Orphanet:3440
Part of
Autosomal dominant diseaseMultiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySyndromic disease
Also known as
Mende syndrome · Van der Hoeve Halbertsma Waardenburg Gualdi syndrome · Waardenburg's syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Waardenburg syndrome type 2 4
Waardenburg-Shah syndrome 3
Waardenburg syndrome 2F
Waardenburg syndrome type 1
Waardenburg syndrome type 3

Rare disease

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