All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01397 IGER IgEresponsiveness, atopic (IGER) 147050 AD - - HAVCR1, IL21R, IL4R, MS4A2, PHF11, PLA2G7, SELP, SPINK5 - autosomal dominant
01967 NETH Netherton syndrome (NETH) 256500 AR 1 1 SPINK5 - -
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