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
02024 ECYT2 erythrocytosis, familial, type 2 (ECYT-2) 263400 AR 2 2 VHL - -
01503 pheochromocytoma pheochromocytoma (susceptibility to) 171300 AD 146 142 MAX, RET, TMEM127, VHL cerebral cortex -
01382 RCC carcinoma, renal cell, nonpapillary (RCC) 144700 - 2 1 DIRC2, FLCN, HNF1A, HNF1B, OGG1, RNF139, VHL - -
01603 VHLS Von Hippel-Lindau syndrome 193300 AD 1 1 CCND1, VHL - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.