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
01246 CMT-2A1 Charcot-Marie-Tooth disease, type 2A1 (CMT-2A1) 118210 - - - KIF1B - -
01970 NBLST-1 neuroblastoma, susceptibility to, type 1 (NBLST-1) 256700 - - - KIF1B, NME1 - -
01503 pheochromocytoma pheochromocytoma 171300 - - - GDNF, KIF1B, MAX, RET, SDHB, SDHD, TMEM127, VHL - -
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