Autoimmune Disease
A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to their own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis).
Genes analysed
Also known as
autoimmune disease or disorder; autoimmune disorder; disease, autoimmune
Includes 265 related subtypes ↓Hide subtypes ↑
- AChR+ myasthenia gravis
- acquired epidermolysis bullosa
- acute inflammatory demyelinating polyradiculoneuropathy
- acute motor and sensory axonal neuropathy
- acute motor axonal neuropathy
- acute pure sensory neuropathy
- acute sensory ataxic neuropathy
- adult-onset myasthenia gravis
- alopecia universalis onychodystrophy vitiligo
- ankylosing spondylitis
- anti-glomerular basement membrane disease
- anti-neutrophil antibody associated vasculitis
- anti-p200 pemphigoid
- antiphospholipid syndrome
- arthus reaction
- atrophic thyroiditis
- autoerythrocyte sensitization syndrome
- autoimmune atherosclerosis
- autoimmune autonomic ganglionopathy
- autoimmune bullous skin disease
- autoimmune cardiomyopathy
- autoimmune cholangitis
- autoimmune disease of ear, nose and throat
- autoimmune disease with susceptibility to mycobacterium tuberculosis
- autoimmune disease, multisystem, infantile-onset
- autoimmune disease, multisystem, infantile-onset, 2
- autoimmune disease, multisystem, infantile-onset, 3
- autoimmune disease, multisystem, infantile-onset, 5
- autoimmune disorder of blood
- autoimmune disorder of cardiovascular system
- autoimmune disorder of central nervous system
- autoimmune disorder of endocrine system
- autoimmune disorder of exocrine system
- autoimmune disorder of gastrointestinal tract
- autoimmune disorder of musculoskeletal system
- autoimmune disorder of peripheral nervous system
- autoimmune disorder of the nervous system
- autoimmune encephalitis
- autoimmune encephalopathy with parasomnia and obstructive sleep apnea
- autoimmune enteropathy
- autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome
- autoimmune enteropathy type 3
- autoimmune epilepsy
- autoimmune gastritis
- autoimmune glomerulonephritis
- autoimmune hemolytic anemia
- autoimmune hemolytic anemia, cold type
- autoimmune hemolytic anemia, warm type
- autoimmune hepatitis
- autoimmune hepatitis type 1
- autoimmune hepatitis type 2
- autoimmune hepatitis type 3
- autoimmune hypoparathyroidism
- autoimmune inner ear disease
- autoimmune limbic encephalitis
- autoimmune lymphoproliferative syndrome
- autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
- autoimmune lymphoproliferative syndrome type 1
- autoimmune lymphoproliferative syndrome type 2A
- autoimmune lymphoproliferative syndrome type 2B
- autoimmune lymphoproliferative syndrome type 4
- autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD
- autoimmune myocarditis
- autoimmune neuropathy
- autoimmune oophoritis
- autoimmune optic neuritis
- autoimmune pancreatitis
- autoimmune pancreatitis type 1
- autoimmune pancreatitis type 2
- autoimmune polyendocrine syndrome type 1
- autoimmune polyendocrinopathy
- autoimmune polyendocrinopathy type 2
- autoimmune polyendocrinopathy type 3
- autoimmune polyendocrinopathy type 4
- autoimmune primary ovarian failure
- autoimmune pulmonary alveolar proteinosis
- autoimmune pulmonary disease due to PD-1 deficiency
- autoimmune retinopathy
- autoimmune thrombocytopenia
- autoimmune thrombocytopenic purpura
- autoimmune thyroid disease
- autoimmune urticaria
- autoimmune uveitis
- autoimmune vasculitis
- autosomal systemic lupus erythematosus type 16
- benign lymphoepithelial lesion of salivary gland
- bullous pemphigoid
- bullous systemic lupus erythematosus
- Castleman-Kojima disease
- catastrophic antiphospholipid syndrome
- celiac disease
- central nervous system lupus
- chilblain lupus
- chilblain lupus 1
- chilblain lupus 2
- chronic childhood arthritis
- chronic cutaneous lupus erythematosus
- chronic progressive multiple sclerosis
- CNS demyelinating autoimmune disease
- Cogan syndrome
- cold agglutinin disease
- CREST syndrome
- cryofibrinogenemia
- cryofibrinogenemia, familial primary
- cryoglobulinemia
- cutaneous lupus erythematosus
- cutaneous pseudolymphoma
- dermatitis herpetiformis
- dermatitis herpetiformis, familial
- diffuse cutaneous systemic sclerosis
- diffuse scleroderma
- discoid lupus erythematosus
- drug-induced autoimmune hemolytic anemia
- drug-induced lupus erythematosus
- eosinophilic angiocentric fibrosis
- euthyroid Graves orbitopathy
- Evans syndrome
- facial diplegia with paresthesias
- familial antiphospholipid syndrome
- familial chilblain lupus
- FAS-related autoimmune lymphoproliferative immune disorder
- Felty syndrome
- fibrosclerosis, multifocal
- generalized myasthenia gravis
- generalized vitiligo
- giant cell hepatitis with autoimmune hemolytic anemia
- Graves disease
- Guillain-Barre syndrome
- Guillain-Barre syndrome, familial
- Hailey-Hailey disease
- Hashimoto thyroiditis
- herpetiform pemphigus
- hypertrophic or verrucous lupus erythematosus
- IgA pemphigus
- IgG4-related aortitis
- IgG4-related dacryoadenitis and sialadenitis
- IgG4-related kidney disease
- IgG4-related mediastinitis
- IgG4-related mesenteritis
- IgG4-related ophthalmic disorder
- IgG4-related pachymeningitis
- IgG4-related retroperitoneal fibrosis
- IgG4-related sclerosing cholangitis
- IgG4-related submandibular gland disease
- IgG4-related thyroid disease
- immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
- immunoglobulin G4-related sclerosing disease
- insulin autoimmune syndrome
- Jaccoud syndrome
- juvenile ankylosing spondylitis
- juvenile dermatitis herpetiformis
- juvenile myasthenia gravis
- juvenile spondyloarthropathy
- Kimura disease
- Lane Hamilton syndrome
- latent autoimmune diabetes in adults
- Libman-Sacks endocarditis
- limited cutaneous systemic sclerosis
- limited systemic sclerosis
- linear IgA Dermatosis
- linear scleroderma
- lipodermatosclerosis
- localized scleroderma
- lupus erythematosus
- lupus erythematosus panniculitis
- lupus erythematosus tumidus
- lymphocytic hypophysitis
- Marburg acute multiple sclerosis
- MASS syndrome
- Miller Fisher syndrome
- mixed connective tissue disease
- mixed-type autoimmune hemolytic anemia
- mucous membrane pemphigoid
- multiple sclerosis
- multisystem autoimmune disease due to IKAROS gain of function
- muscle-specific tyrosine kinase-associated myasthenia gravis
- myasthenia gravis
- myasthenia gravis with thymus hyperplasia
- myasthenia, limb-girdle, autoimmune
- neonatal antiphospholipid syndrome
- neonatal autoimmune hemolytic anemia
- neonatal dermatomyositis
- neonatal lupus erythematosus
- neonatal myasthenia gravis
- neonatal scleroderma
- non-specific autoimmune brainstem encephalitis with characteristic antibodies
- non-specific autoimmune brainstem encephalitis without characteristic antibodies
- non-specific autoimmune cerebellar ataxia with characteristic antibodies
- non-specific autoimmune cerebellar ataxia without characteristic antibodies
- non-specific autoimmune supratentorial encephalitis with characteristic antibodies
- non-specific autoimmune supratentorial encephalitis without characteristic antibodies
- ocular cicatricial pemphigoid
- ocular myasthenia gravis
- overlapping connective tissue disease
- PANDAS
- paraneoplastic pemphigus
- paraparetic variant of Guillain-Barre syndrome
- paroxysmal cold hemoglobinuria
- pediatric acute-onset neuropsychiatric syndrome
- pediatric multiple sclerosis
- pediatric systemic lupus erythematosus
- pediatric-onset Graves disease
- pemphigoid
- pemphigoid gestationis
- pemphigus
- pemphigus and fogo selvagem
- pemphigus erythematosus
- pemphigus foliaceus
- pemphigus vegetans
- pemphigus vulgaris
- pharyngeal-cervical-brachial variant of Guillain-Barre syndrome
- polyarticular juvenile rheumatoid arthritis
- polyneuropathy, inflammatory demyelinating, chronic
- postpartum thyroiditis
- primary antiphospholipid syndrome
- primary autoimmune enteropathy
- primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome
- primary cutaneous plasmacytosis
- primary progressive multiple sclerosis
- primary thrombocytopenia
- progressive relapsing multiple sclerosis
- psoriasis-related juvenile idiopathic arthritis
- psoriatic arthritis
- pulmonary systemic sclerosis
- relapsing-remitting multiple sclerosis
- Reynolds syndrome
- rheumatic fever
- rheumatic pulmonary valve disease
- rheumatoid arthritis
- rheumatoid arthritis-associated interstitial lung disease
- rheumatoid vasculitis
- Rowell syndrome
- scleroderma
- scleroderma, familial progressive
- secondary antiphospholipid syndrome
- secondary neonatal autoimmune disease
- secondary progressive multiple sclerosis
- seronegative autoimmune hepatitis
- seronegative myasthenia gravis
- serum sickness
- severe autoimmune neutropenia
- Sjogren syndrome
- STAT3-related early-onset multisystem autoimmune disease
- steroid-responsive encephalopathy associated with autoimmune thyroiditis
- subacute cutaneous lupus erythematosus
- subcorneal pustular dermatosis
- Susac syndrome
- systemic lupus erythematosus
- systemic lupus erythematosus 17
- systemic lupus erythematosus 18
- systemic lupus erythematosus related to C1QA
- systemic lupus erythematosus related to C1QB
- systemic lupus erythematosus related to C1QC
- systemic lupus erythematosus related to C1S
- systemic lupus erythematosus related to C4A
- systemic sclerosis
- tempi syndrome
- transient neonatal myasthenia gravis
- trichrome vitiligo
- type 1 diabetes mellitus
- type 3 autoimmune lymphoproliferative syndrome
- type II hypersensitivity reaction disease
- type III hypersensitivity disease
- undifferentiated connective tissue syndrome
- vitiligo
