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
07107 AMC5 arthrogryposis multiplex congenita, type 5 618947 AR - - TOR1A - -
00369 DYT1 dystonia, torsion, early onset, type 1 (DYT-1) 128100 AD 5 5 TOR1A - -
05265 MRRSDC;LGMD2Y dystrophy, dystrophy, autosomal recessive, with rigid spine and distal joint contractures (LGMD2Y) 617072 AR 1 1 TOR1AIP1 - -
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