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
05352 BCS cornea, brittle, syndrome (BCS) - - 16 16 PRDM5, ZNF469 - -
03570 BCS2 cornea, brittle, syndrome type 2 (BCS-2) 614170 AR 3 3 PRDM5 - -
00169 EDS Ehlers-Danlos syndrome (EDS) - - 1800 241 ADAMTS2, B4GALT7, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, FKBP14, PLOD1, PRDM5, SLC39A13, TNXB - -
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