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
00161 ECYT2 Erythrocytosis, familial, 2 263400 - 0 0 VHL - -
00087 Pheo Pheochromocytoma, susceptibility to 171300 - 23 23 MAX, RET, SDHB, SDHD, TMEM127, VHL - -
00162 VHL von Hippel-Lindau syndrome 193300 - 0 0 VHL - -
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