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4 entries on 1 page. Showing entries 1 - 4.
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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 - -
00001 ALXDRD Alexander Disease 203450 - 142 41 GFAP - -
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 - -
00029 PD Parkinson Disease 168600 - 558 1 ADORA1, DNAJC13, FBXO7, LRRK2, MAPT, PARK2, PARK7, PINK1, PODXL, PRNP, PTRHD1, RIC3, SNCA, SYNJ1, VPS35 - -
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