All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00638 - Ehlers-Danlos syndrome, cardiac valvular form 225320 - - - COL1A2 - -
01484 - osteoporosis 166710 - - - CALCR, COL1A1, COL1A2, LRP5, PDLIM4, VDR - -
00169 EDS Ehlers-Danlos syndrome 130000 - - - ADAMTS2, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, FKBP14, PLOD1, TNXB - -
00634 EDS-7B Ehlers-Danlos syndrome, type VIIB (EDS-7B) 130060 - - - COL1A1, COL1A2 - -
00637 OI-2 osteogenesis imperfecta, type II (OI-2) 166210 - - - COL1A1, COL1A2 - -
00636 OI-3 osteogenesis imperfecta, type III (OI-3) 259420 - - - COL1A1, COL1A2 - -
00635 OI-4 osteogenesis imperfecta, type IV (OI-4) 166220 - - - COL1A1, COL1A2 - -
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