- Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
- Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR1 deficiency
a selection of possible paths
SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of immune function 414029004
Immunodeficiency disorder 234532001
Primary immune deficiency disorder 58606001
Immunodeficiency associated with chromosomal abnormality 234632005
Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency 718230004
SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency 718230004
sorted most to least specific