All diseases

11 entries on 1 page. Showing entries 1 - 11.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06885 AMD dysplasia, acromesomelic - - 2 2 BMPR1B, GDF5, NPR2, PRKG2 - -
00191 AMD2A dysplasia, acromesomelic, type 2A, Grebe 200700 AR 3 3 GDF5 - -
01034 AMD2B dysplasia, acromesomelic, type 2B, Du Pan syndrome 228900 AR 0 0 GDF5 - -
01032 AMD2C dysplasia, acromesomelic, type 2C, Hunter-Thompson 201250 AR 0 0 GDF5 - -
03821 BDA1C brachydactyly, type A1, C (BD-A1C) 615072 AR 0 0 GDF5 - -
00184 BDA2 brachydactyly, type A2 (BD-A2) 112600 AD 0 0 BMP2, BMPR1B, GDF5 - -
01033 BDC brachydactyly, type C (BD-C) 113100 AD 3 1 GDF5 - -
01036 OS5 sosteoarthritis, susceptibility 5 (OS-5) 612400 - 0 0 GDF5 - -
00729 SYM symphalangism, proximal (SYM) - - 12 11 GDF5, NOG - -
03892 SYM1B symphalangism, proximal, type 1B (SYM1B) 615298 AD 0 0 GDF5 - -
01035 SYNS2 synostoses syndrome, multiple, type 2 (SYNS-2) 610017 AD 1 0 GDF5 - -
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