Catalog
Autosomal recessive mendelian susceptibility to mycobacterial diseases
No MMS code
Link to WHO Definition
Autosomal recessive mendelian susceptibility to mycobacterial diseases – http://id.who.int/icd/entity/2128441981
This refers to the autosomal recessive illness caused by abnormalities in genes or chromosomes, with susceptibility to mycobacterial diseases.
Parents
Children
- Complete autosomal recessive interferon-gamma receptor 2 deficiency
- Autosomal recessive interleukin 12 receptor beta-1 chain deficiency
- Autosomal recessive tyrosine kinase 2 deficiency
- Complete autosomal recessive interferon-gamma receptor 1 deficiency
- Partial autosomal recessive interferon-gamma receptor 1 deficiency
- Partial autosomal recessive interferon-gamma receptor 2 deficiency
- Autosomal recessive interleukin 12p40 deficiency