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Waardenburg syndrome type 2

Disease Export to PDF
Name:
Waardenburg syndrome type 2
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.
ORPHAcode:
895
Synonyms:
WS2
Waardenburg syndrome type II
XREF(s):
Orphanet
OMIM
OMIM
OMIM
OMIM
OMIM
OMIM
MeSH
ICD-10
Analyte(s):
KITLG
TYR
SNAI2
SOX10
MITF
EDNRB
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14