Parent term(s)
primary immunodeficiency disease
+
Term with siblings
autoimmune disease +
autoinflammation, antibody deficiency, and immune dysregulation syndrome
autosomal dominant familial periodic fever
B cell deficiency
+
combined immunodeficiency
+
complement deficiency
+
dendritic cell deficiency
+
ectodermal dysplasia and immune deficiency
+
epidermodysplasia verruciformis
familial Behcet-like autoinflammatory syndrome
familial cold autoinflammatory syndrome
+
immunodeficiency 18
immunodeficiency 20
immunodeficiency 21
immunodeficiency 27A
immunodeficiency 27B
immunodeficiency 28
immunodeficiency 29
immunodeficiency 31A
immunodeficiency 31B
immunodeficiency 31C
immunodeficiency 35
immunodeficiency 38
immunodeficiency 39
immunodeficiency 42
immunodeficiency 43
immunodeficiency 44
immunodeficiency 45
immunodeficiency 47
immunodeficiency 51
immunodeficiency 57
immunodeficiency 65
immunodeficiency 66
lymphoproliferative syndrome
+
NK cell deficiency
+
phagocyte bactericidal dysfunction
+
T cell and NK cell immunodeficiency
+
T cell deficiency
+
WHIM syndrome 1
WHIM syndrome 2
Child term(s)
antisynthetase syndrome
autoimmune disease of blood
+
autoimmune disease of cardiovascular system
+
autoimmune disease of endocrine system
+
autoimmune disease of exocrine system
+
autoimmune disease of gastrointestinal tract
+
autoimmune disease of musculoskeletal system
+
autoimmune disease of the nervous system
+
autoimmune disease of urogenital tract
+
autoimmune interstitial lung, joint, and kidney disease
CINCA Syndrome
common variable immunodeficiency
+
familial Mediterranean fever
Felty's syndrome
IgG4-related disease
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
Jaccoud's syndrome
Mikulicz disease
PFAPA syndrome
denotes an 'is-a' relationship