Cytoscape Web
Click node...

Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Takayasu arteritis
Primary biliary cirrhosis
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
Behçet disease
Synonym(s):
- MSMD due to complete IL12B deficiency
- MSMD due to complete interleukin 12B deficiency
- Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
IL12B P29460161561
No signs/symptoms info available.