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Any hereditary predisposition to infections in which the cause of the disease is a mutation in the TYK2 gene.
Features include: Increased circulating IgE concentration, Recurrent mycobacterial infections, Recurrent viral infections, and Recurrent respiratory infections and 2 more.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Blood and immune system | 5 | Recurrent mycobacterial infections, Recurrent viral infections, Recurrent respiratory infections |
Lab test results | 1 | Increased circulating IgE concentration |
Lungs and breathing | 1 | Recurrent respiratory infections |
TYK2 function has not been fully characterized.
Immunodeficiency 35 is associated with mutations in the TYK2 gene on chromosome 19.
Genetic testing for TYK2 is available. Testing is considered confirmatory for diagnosis.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for immunodeficiency 35.
12 publications have been identified in PubMed for immunodeficiency 35. Research spans Basic Science / Preclinical (42%), Case Report / Case Series (33%), and Other (8%).
Research Type | Count | % of Total |
|---|---|---|
Laboratory research | 5 | 42% |
Patient case studies | 4 | 33% |
Other research | 1 | 8% |
Research summaries | 1 | 8% |
Disease patterns and progression | 1 | 8% |
Hafsi W (2026). [PMID: 30247822](https://pubmed.ncbi.nlm.nih.gov/30247822/). *Unknown Journal*. [Case Report / Case Series]
Hennighausen L (2025). [PMID: 41327031](https://pubmed.ncbi.nlm.nih.gov/41327031/). *BMC Genomics*. [Basic Science / Preclinical]
Gastaldi T (2025). [PMID: 40530418](https://pubmed.ncbi.nlm.nih.gov/40530418/). *iScience*. [Basic Science / Preclinical]
Xie L (2025). [PMID: 40586332](https://pubmed.ncbi.nlm.nih.gov/40586332/). *Int J Immunopathol Pharmacol*. [Review / Meta-Analysis]
Karjalainen A (2025). [PMID: 40025196](https://pubmed.ncbi.nlm.nih.gov/40025196/). *Cell Mol Life Sci*. [Basic Science / Preclinical]
Sikhayeva N (2025). [PMID: 41465118](https://pubmed.ncbi.nlm.nih.gov/41465118/). *Genes (Basel)*. [Case Report / Case Series]
Alimi A (2025). [PMID: 40949057](https://pubmed.ncbi.nlm.nih.gov/40949057/). *J Hum Immun*. [Case Report / Case Series]
Johnson B (2024). [PMID: 39403378](https://pubmed.ncbi.nlm.nih.gov/39403378/). *Front Immunol*. [Basic Science / Preclinical]
Gao Y (2024). [PMID: 38896258](https://pubmed.ncbi.nlm.nih.gov/38896258/). *J Clin Immunol*. [Case Report / Case Series]
Obeidat L (2024). [PMID: 39268404](https://pubmed.ncbi.nlm.nih.gov/39268404/). *Biomed Rep*. [Epidemiology / Natural History]
Data assembled from 6 of 12 sources · Last updated Sep 19, 2026, 2:00 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center