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
05349 CGD granulomatous disease, chronic - - 1322 1305 C17orf62, CYBA, CYBB, NCF1, NCF2, NCF4 - -
01831 CGD1 granulomatous disease, chronic, due to deficiency of NCF-1, type 1 233700 AR - - NCF1 - -
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