All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01768 SHFM6 split-hand/foot malformation, type 6 (SHFM-6) 225300 AR 6 6 WNT10B - -
05251 STHAG8 agenesis, tooth, selective, type 8 (STHAG-8) 617073 AD - - WNT10B - -
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