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
02785 - Spondyloepimetaphyseal dysplasia Matrilin-3 related 608728 AR 1 1 MATN3 - -
02626 EDM5 dysplasia, epiphyseal, multiple, type 5 (EDM-5) 607078 AD 50 14 MATN3 - -
01359 OS2 sosteoarthritis, susceptibility 2 (OS-2) 140600 AD 2 1 MATN3 - -
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