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
01829 CCHIDG immune defects, combined cellular and humoral with granulomas (CCHIDG) 233650 AR - - RAG1, RAG2 - -
02460 Omenn Omenn syndrome 603554 AR 20 2 DCLRE1C, RAG1, RAG2 - -
02363 SCIDN immunodeficiency, severe combined, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive 601457 AR 8 - RAG1, RAG2 - -
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