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
04255 ALS sclerosis, lateral, amyotrophic (ALS) - - 471 442 GLE1, LRP12, PFN1 - -
07019 ALS28 sclerosis, lateral, amyotrophic 620452 AD - - LRP12 - -
03051 FCAS2 autoinflammatory syndrome, cold, familial, type 2 (FCAS-2) 611762 AD - - NLRP12 - -
05741 OPDM myopathy, oculopharyngodistal (OPDM) - - 60 43 GIPC1, LRP12, NOTCH2NLC, RILPL1 - -
05742 OPDM1 myopathy, oculopharyngodistal, type 1 (OPDM1) 164310 AD;AR - - LRP12 - -
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