Immune System Diseases | Page 1

2 Diseases

22q11.2 deletion syndrome

A Diseases

Adenosine Deaminase 2 deficiency Adenosine deaminase deficiency Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies Agammaglobulinemia, non-Bruton type Aicardi-Goutieres syndrome Allergic bronchopulmonary aspergillosis Alopecia areata Alopecia totalis Alopecia universalis Amyloidosis AA Amyloidosis familial visceral Ataxia telangiectasia Autoimmune lymphoproliferative syndrome Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency Autoimmune polyglandular syndrome type 1 Autosomal dominant hyper IgE syndrome Autosomal recessive candidiasis familial chronic mucocutaneous Autosomal recessive early-onset inflammatory bowel disease Autosomal recessive hyper IgE syndrome

B Diseases

Bare lymphocyte syndrome 2 Barth syndrome Blau syndrome Bloom syndrome Bronchiolitis obliterans

C Diseases

C1q deficiency Cartilage-hair hypoplasia CHARGE syndrome Chediak-Higashi syndrome Cherubism Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature Chronic graft versus host disease Chronic granulomatous disease Cohen syndrome Combined immunodeficiency with skin granulomas Common variable immunodeficiency Complement component 2 deficiency Complement component 8 deficiency type 1 Complement component 8 deficiency type 2 Congenital pulmonary alveolar proteinosis Cryoglobulinemia Cutaneous mastocytoma Cyclic neutropenia

D Diseases

Deficiency of interleukin-1 receptor antagonist Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Dyskeratosis congenita Dyskeratosis congenita autosomal dominant Dyskeratosis congenita autosomal recessive Dyskeratosis congenita X-linked

E Diseases

Epidermodysplasia verruciformis

F Diseases

Familial amyloidosis, Finnish type Familial cold autoinflammatory syndrome Familial hemophagocytic lymphohistiocytosis Familial Mediterranean fever Familial mixed cryoglobulinemia Familiar chronic mucocutaneous candidiasis Felty's syndrome

G Diseases

Glycogen storage disease type 1B Griscelli syndrome type 2

H Diseases

Hashimoto encephalopathy Hashimoto's syndrome Hennekam syndrome Hepatic venoocclusive disease with immunodeficiency Hereditary folate malabsorption Hermansky Pudlak syndrome 2 Herpes simplex encephalitis Hoyeraal Hreidarsson syndrome Hyper-IgD syndrome Hyper IgE syndrome

I Diseases

ICF syndrome Idiopathic acute eosinophilic pneumonia Idiopathic CD4 positive T-lymphocytopenia IL12RB1 deficiency Immune defect due to absence of thymus Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Immunodeficiency with hyper IgM type 1 Immunodeficiency with hyper IgM type 2 Immunodeficiency with hyper IgM type 3 Immunodeficiency with hyper IgM type 4 Immunodeficiency with hyper IgM type 5 Immunodeficiency without anhidrotic ectodermal dysplasia Immunodeficiency with thymoma Immunodysregulation, polyendocrinopathy and enteropathy X-linked Immunoglobulin A deficiency 2 Intestinal atresia multiple IRAK-4 deficiency Isolated growth hormone deficiency type 3

K Diseases

Kawasaki disease

L Diseases

Lambert Eaton myasthenic syndrome Leukocyte adhesion deficiency type 1 LRBA deficiency Lupus Lymphocytic hypophysitis

M Diseases

Majeed syndrome Melkersson-Rosenthal syndrome MHC class 1 deficiency Muckle-Wells syndrome Multifocal fibrosclerosis Multiple sclerosis