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
02982 - Immunodeficiency due to defect in mapbp-interacting protein 610798 AR - - LAMTOR2 - -
02650 FCORD2 dysplasia, cortical, focal type II (FCORD-2) 607341 - 4 - MTOR, TSC1, TSC2 - -
05548 SKS Smith-Kingsmore syndrome (SKS) 616638 AD 2 1 MTOR - autosomal dominant
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