All diseases

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01603 - Von Hippel-Lindau syndrome 193300 - - - CCND1, VHL - -
02024 ECYT-2 erythrocytosis, familial, type 2 (ECYT-2) 263400 - - - VHL - -
01503 pheochromocytoma pheochromocytoma 171300 - - - GDNF, KIF1B, MAX, RET, SDHB, SDHD, TMEM127, VHL - -
01382 RCC carcinoma, renal cell, nonpapillary (RCC) 144700 - - - DIRC2, FLCN, HNF1A, HNF1B, OGG1, RNF139, VHL - -
Legend   How to query