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
02460 Omenn Omenn syndrome 603554 AR 20 2 DCLRE1C, RAG1, RAG2 - -
00988 RSSCID immunodeficiency, severe combined, Athabascan type 602450 AR 2 2 DCLRE1C, LIG4 - -
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