Disease #02799 (WS2D (Waardenburg syndrome, type 2D (WS2D)), OMIM:608890)

Official abbreviation WS2D
Name Waardenburg syndrome, type 2D (WS2D)
OMIM ID 608890
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease -
Associated with 1 gene SNAI2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00415812 S-5 - - M ? China Chinese - - - - WS2D - SOX10 SOX10 1 1 Jian Song
00415815 S-6 - - F no China Chinese - - - - WS2D - SOX10 SOX10 1 1 Jian Song
00415816 S-8 - - F no China Chinese - - - - WS2D - SOX10 SOX10 1 1 Jian Song
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