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Diseases

Genetic and Rare Diseases Information Center (GARD)

Search for Rare or Genetic Diseases


Immune System Diseases

* This symbol indicates that a condition is not rare but is one for which a question has been answered by the GARD Information Center.

Is Rare Condition? Disease Name
* 22q11.2 deletion syndrome
* Adenosine deaminase deficiency
* Allergic bronchopulmonary aspergillosis
*   Alopecia areata
*   Alopecia totalis
* Alopecia universalis
* Amyloidosis AA
* Amyloidosis familial visceral
* Ataxia telangiectasia
* Autoimmune lymphoproliferative syndrome
* Autoimmune polyglandular syndrome type 1
* Autosomal dominant hyper IgE syndrome
* Autosomal recessive hyper IgE syndrome
* Bare lymphocyte syndrome 2
* Barth syndrome
* Blau syndrome
* Bloom syndrome
* Candidiasis familial chronic mucocutaneous, autosomal recessive
* Cartilage-hair hypoplasia
* Chediak-Higashi syndrome
* Chronic granulomatous disease
* Chronic Infantile Neurological Cutaneous Articular syndrome
* Cohen syndrome
* Common variable immunodeficiency
* Complement component 8 deficiency type 1
* Complement component 8 deficiency type 2
* Congenital disorder of glycosylation type 2C
* Cryoglobulinemia
* Cryoglobulinemia, familial mixed
* Cyclic neutropenia
* Deficiency of interleukin-1 receptor antagonist
* Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency
* Dyskeratosis congenita
* Dyskeratosis congenita autosomal dominant
* Epidermodysplasia verruciformis
* Familial amyloidosis, Finnish type
* Familial cold autoinflammatory syndrome
* Familial Mediterranean fever
* Felty's syndrome
* Glycogen storage disease type 1B
* Griscelli syndrome type 2
* Hashimoto's encephalitis
*   Hashimoto's syndrome
* Hepatic venoocclusive disease with immunodeficiency
* Hermansky Pudlak syndrome 2
* Hoyeraal Hreidarsson syndrome
* Hyper IgE syndrome
* Hyper-IgD syndrome
* ICF syndrome
* Idiopathic acute eosinophilic pneumonia
* 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
* Immunodysregulation, polyendocrinopathy and enteropathy X-linked
* Immunoglobulin A deficiency 2
* IRAK-4 deficiency
* Kawasaki syndrome
* Large granular lymphocyte leukemia
*   Lupus
* Lymphocytic hypophysitis
* Majeed syndrome
* Melkersson-Rosenthal syndrome
* MHC class 1 deficiency
* Muckle-Wells syndrome
* Multifocal fibrosclerosis
*   Multiple sclerosis
* Neonatal systemic lupus erythematosus
* Neutrophil-specific granule deficiency
* Nijmegen breakage syndrome
* Omenn syndrome
* Osteopetrosis autosomal recessive 7
*   Palindromic rheumatism
* Papillon Lefevre syndrome
* Partial androgen insensitivity syndrome
* Pearson syndrome
* Pediatric multiple sclerosis
* Periodic fever, aphthous stomatitis, pharyngitis and adenitis
* Periodic fever, familial, autosomal dominant
* Poikiloderma with neutropenia
* Pruritic urticarial papules plaques of pregnancy
* Purine nucleoside phosphorylase deficiency
* Pyogenic arthritis, pyoderma gangrenosum and acne
* Relapsing polychondritis
* Reticular dysgenesis
*   Sarcoidosis
* Say Barber Miller syndrome
* Selective IgA deficiency
* Severe combined immunodeficiency
* Severe combined immunodeficiency with sensitivity to ionizing radiation
* Severe combined immunodeficiency, atypical
* Severe congenital neutropenia autosomal recessive 3
* Severe congenital neutropenia X-linked
* Severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive
* Shwachman-Diamond syndrome
* Spondyloenchondrodysplasia
* Stevens-Johnson syndrome
* TARP syndrome
* Twin twin transfusion syndrome
* Vici syndrome
* WHIM syndrome
* Wiskott Aldrich syndrome
* Woods Black Norbury syndrome
* X-linked agammaglobulinemia
* X-linked lymphoproliferative syndrome
* X-linked lymphoproliferative syndrome 1
* X-linked lymphoproliferative syndrome 2
* X-linked magnesium deficiency with Epstein-Barr virus infection and neoplasia
* X-linked severe combined immunodeficiency
* ZAP-70 deficiency