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
06586 EIEE73 Epileptic encephalopathy, early infantile, 73 618379 AD - - RNF13 - -
00722 MMFD macrocephaly, macrosomia, facial dysmorphism syndrome (MMFD) 614192 - 9 9 RNF135 - -
01382 RCC carcinoma, renal cell, nonpapillary (RCC) 144700 - 2 1 DIRC2, FLCN, HNF1A, HNF1B, OGG1, RNF139, VHL - -
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