All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01979 OODD dysplasia, odontoonychodermal (OODD) 257980 AR 0 0 WNT10A - -
01762 SSPS Schopf-Schulz-Passarge syndrome (SSPS) 224750 AR 2 2 WNT10A - -
01411 STHAG4 agenesis, tooth, selective, type 4 (STHAG-4) 150400 AD;AR 1 1 WNT10A - -
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