Disease & disorder
Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
MONDO:0013954
Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the IL12B gene.
Outbreak surveillance
Global reported eventsExplore recent public health notices potentially related to Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency. Results are keyword matches, not yet verified disease-to-outbreak relationships.
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Background context
Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.Drugs being studied
Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.