Waardenburg syndrome type 2

MONDO:0019517

Waardenburg 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

1 clinical trial for this condition and its sub-types, 1 tagged with Waardenburg syndrome type 2 itself.

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Sub-types of Waardenburg syndrome type 2

Including sub-types (1) Tagged with Waardenburg syndrome type 2 (1)

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Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC

Waardenburg syndrome type 2

Where it sits in the disease tree

Newborn screening study aims to catch rare diseases at birth