Autosomal dominant Stat1 deficiency (Q106061): Difference between revisions
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Revision as of 12:50, 17 August 2026
Mendelian susceptibility to mycobacterial diseases (MSMD) due to partial STAT1 (signal transducer and activator of transcription 1) deficiency is a genetic variant of MSMD characterised by a partial defect in the interferon (IFN)-gamma pathway, leading to mild mycobacterial infections.
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| default for all languages | ID_2037189455 |
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| English | Autosomal dominant Stat1 deficiency |
Mendelian susceptibility to mycobacterial diseases (MSMD) due to partial STAT1 (signal transducer and activator of transcription 1) deficiency is a genetic variant of MSMD characterised by a partial defect in the interferon (IFN)-gamma pathway, leading to mild mycobacterial infections. |
