Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency

Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder)

active

Code	`725151007`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20170731

Synonyms

Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency

Parents (2)

11164009Autosomal dominant hereditary disorder disorder
1172895006Mendelian susceptibility to mycobacterial disease disorder

Children (0)

None (leaf concept).