All diseases

10 entries on 1 page. Showing entries 1 - 10.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01032 - Acromesomelic dysplasia, Hunter-Thompson type 201250 - 0 0 GDF5 - -
01034 - Fibular hypoplasia and complex brachydactyly 228900 - 0 0 GDF5 - -
00191 AMDG chondrodysplasia, acromesomelic, type Grebe (AMDG) 200700 - 3 3 BMPR1B, GDF5 - -
03821 BD-A1C brachydactyly, type A1, C (BD-A1C) 615072 - 0 0 GDF5 - -
00184 BD-A2 brachydactyly, type A2 (BD-A2) 112600 - 0 0 BMP2, BMPR1B, GDF5 - -
01033 BD-C brachydactyly, type C (BD-C) 113100 - 3 1 GDF5 - -
01036 OS-5 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 SYNS-2 synostoses syndrome, multiple, type 2 (SYNS-2) 610017 - 1 0 GDF5 - -
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