Waardenburg syndrome type 2
Name: |
Waardenburg syndrome type 2
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Description: |
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.
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ORPHAcode: |
895
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Synonyms: |
WS2
Waardenburg syndrome type II
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
22 Jun 2023 - 16:14
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