All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06662 DMRV Myopathy, distal, with rimmed vacuoles 617158 AD 1 1 SQSTM1 - -
04673 FTDALS3 dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 3 (FTDALS-3) 616437 AD - - SQSTM1 - -
06661 NADGP Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset 617145 AR - - SQSTM1 - -
04674 PDB3 Paget disease of bone, type 3 (PDB-3) 167250 AD - - SQSTM1 - -
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