All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00606 - mitochondrial respiratory chain complex II deficiency 252011 - 0 0 SDHA, SDHAF1, SDHD - -
01222 - tumor, carcinoid, intestinal 114900 - 0 0 SDHD - -
02614 - paraganglioma, gastric stromal sarcoma 606864 - 0 0 SDHB, SDHC, SDHD - -
03829 CWS-3 Cowden syndrome, type 3 (CWS-3) 615106 - 0 0 SDHD - -
01489 PGL-1 paragangliomas, type 1 (PGL-1) 168000 - 211 211 SDHD - -
01503 pheochromocytoma pheochromocytoma 171300 - 146 142 GDNF, KIF1B, MAX, RET, SDHB, SDHD, TMEM127, VHL - -
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