All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04061 RHDA2 hypodysplasia/aplasia, renal, type 2 (RHDA-2) 615721 AR 0 0 FGF20 - -
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