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
00003 ALS Amyotrophic Lateral Sclerosis 105400 - 1029 508 ALS2, ANG, ANXA11, APEX1, ARHGEF28, C9orf72, CCNF, CHCHD10, CHGB, CHMP2B, CYLD, DCTN1, DNAJC7, DPYSL3, ERLIN1, FUS, GLE1, GRN, HFE, HNRNPA1, 34 more - -
00010 FTLD Frontotemporal Lobar Degeneration 607485 - 355 3 CCNF, CHCHD10, CHMP2B, CYLD, FUS, GFAP, GRN, GSK3B, LRRK2, MAPT, NEK1, NOTCH3, OPTN, PRNP, PSEN1, SOD1, SQSTM1, TARDBP, TBK1, TREM2, UBQLN2, VCP - -
00031 PBP Progressive Bulbar Palsy - - 3 - SOD1, TTR - -
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