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
01960 - myosclerosis, autosomal recessive 255600 AR - - COL6A2 - -
05358 BTHLM myopathy, Bethlem (BTHLM) - - 38 38 COL12A1, COL6A1, COL6A2, COL6A3 - -
07176 BTHLM1B myopathy, Bethlem, type 1B 620725 AD;AR - - COL6A2 - -
01945 UCMD dystrophy, muscular, congenital, Ullrich - AD;AR;Di 8 7 COL6A1, COL6A2, COL6A3 - -
07178 UCMD1B dystrophy, Uhlrich, muscular, congenital, type 1B 620727 AD;AR;Di - - COL6A2 - -
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