Parent term(s)
primary immunodeficiency disease
+
Term with siblings
complement deficiency +
autoimmune disease
+
autoinflammation, antibody deficiency, and immune dysregulation syndrome
autosomal dominant familial periodic fever
B cell deficiency
+
combined immunodeficiency
+
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)
atypical hemolytic-uremic syndrome
C1 inhibitor deficiency
complement component 2 deficiency
complement component 3 deficiency
complement component 4a deficiency
complement component 4b deficiency
complement component 5 deficiency
complement component 6 deficiency
complement component 7 deficiency
complement component 9 deficiency
complement factor I deficiency
type I complement component 8 deficiency
type II complement component 8 deficiency
X-linked properdin deficiency
denotes an 'is-a' relationship