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
02020 - alpha-2-plasmin inhibitor deficiency 262850 AR - - SERPINF2 - -
03652 CMTDIE Charcot-Marie-Tooth disease, dominant intermediate, type E (CMTDIE) 614455 AD - - INF2 - -
03511 DKCA3 dyskeratosis congenita, autosomal dominant, type 3 (DKCA-3) 613990 AD 18 18 TINF2 - -
03289 FSGS5 glomerulosclerosis, segmental, focal, type 5 (FSGS-5) 613237 - 1 1 INF2 - -
02055 Revesz Revesz syndrome 268130 AD 2 2 TINF2 - -
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