All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06058 DFNA37 ?Deafness, autosomal dominant 37 618533 AD - - COL11A1 - -
00553 FBCG1 fibrochondrogenesis, type 1 (FBCG-1) 228520 AR - - COL11A1 - -
02474 IDD intervertebral disc disease (IDD) 603932 - 2 - ASPN, CILP, COL11A1, COL9A2, COL9A3, THBS2 - -
00552 MRSHS Marshall syndrome (MRSHS) 154780 AD 2 1 COL11A1 - -
00551 STL2 Stickler syndrome, type II (STL-2) 604841 AD 2 2 COL11A1 - -
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