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
00577 DRS Robinow syndrome, autosomal dominant (DRS) - AD 10 9 DVL1, DVL3, WNT5A - -
04454 DRS2 Robinow, autosomal dominant syndrome, type 2 (DRS2) 616331 AD 3 3 DVL1 - -
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