Malattia autoimmune
Un disturbo derivante dalla perdita di funzione o dalla distruzione tissutale di uno o più organi, causato da risposte immunitarie umorali o cellulari dell'individuo dirette contro i costituenti dei propri tessuti. Può essere sistemico (ad es. lupus eritematoso sistemico) oppure organo-specifico (ad es. tiroidite).
Geni analizzati
Conosciuto anche come
autoimmune disease or disorder; autoimmune disorder; disease, autoimmune
Include 265 sottotipi correlati ↓Nascondi i sottotipi ↑
- 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
