Мы используем файлы cookie.
Продолжая использовать сайт, вы даете свое согласие на работу с этими файлами.
List of autoimmune diseases
Другие языки:

List of autoimmune diseases

Подписчиков: 0, рейтинг: 0

This list of autoimmune diseases is categorized by organ and tissue type to help locate diseases that may be similar.

Autoimmune diseases qualifiers

Overview of the qualifiers for the list.

Other Qualifiers
A "Accepted" in prior version of this table.
C A disease, regarded as autoimmune, that is often found in individuals with another autoimmune condition. This designation is given to diseases that are classified by Rose and Bona as having "circumstantial" evidence of autoimmune etiology. Diseases in this list with a "C" are, therefore, actual autoimmune diseases, rather than comorbid symptoms, which appear after this list.
E Disease is an autoimmune response triggered by a specific environmental factor.
F Disease is only caused by autoimmunity in only a fraction of those who have it.
I Described as an autoinflammatory disease.
L Evidence to indicate autoimmunity is extremely limited or circumstantial.
M Disease appears under Autoimmune Diseases in MeSH.
N Not listed in prior version of this table.
R Disease appeared in prior version but has been renamed. In renaming, precedence has been given to scientific names over those based on discoverers.
S "Suspected" in the prior version of this table.
T Disease has a known trigger, such as viral infection, vaccination, or injury.
X An extremely rare disease, which would suggest limited opportunity to study it and conclusively determine whether it is caused by autoimmunity.
Y Listed in the prior version of this table with "Accepted/Suspected" left blank.

Autoimmune diseases

Major organs

Organ/Tissue type

Disease name

Level of acceptance for autoimmunity Hypersensitivity

(I,II,III,IV)

ICD-9

Codes

Notes/Autoantibodies/Synonyms/Rare variants
Heart
Myocarditis Moderate, F, R, A 391.2422429.0 Synonyms: Autoimmune myocarditis, Autoimmune cardiomyopathy, Coxsackie myocarditis
Postmyocardial infarction syndrome Limited, R, Y 411.0 Autoantibodies: Myocardial neo-antigens formed as a result of the MI.
Synonym: Dressler's syndrome
Postpericardiotomy syndrome Limited, N 429.4
Subacute bacterial endocarditis (SBE) Limited, Y III 421.0 Autoantibodies: essential mixed cryoglobulinemia.
Kidney
Anti-Glomerular Basement Membrane nephritis Moderate, R, M, A II 446.21 Autoantibodies: Anti-Basement Membrane Collagen Type IV Protein.
Synonyms: Goodpastures Syndrome, Glomerulonephritis Type 1
Lupus nephritis Comorbidity, N 583.81 A comorbidity of Systemic Lupus Erythematosus.
Bladder
Interstitial cystitis Limited, S 595.1 Mast cells.
Liver
Autoimmune hepatitis Moderate, A cell-mediated 571.42 Autoantibodies: ANA and SMA, LKM-1, LKM-2 or LKM-3; antibodies against soluble liver antigen (anti-SLA, anti-LP) no autoantibodies detected (~20%).
Synonym: Lupoid hepatitis
Primary biliary cholangitis (PBC) Moderate, A 571.6 Autoantibodies: Anti-p62, Anti-sp100, Anti-Mitochondrial(M2), Anti-Ro aka SSA.
Sjogren's is classified in some places (e.g. MeSH) as rheumatoid disease, but there is no published evidence to support that classification.
Primary sclerosing cholangitis Limited, Y 576.1 Possible overlap with primary biliary cirrhosis.
Autoantibodies: HLA-DR52a.
Lung
Antisynthetase syndrome Limited, Y 279.49 Autoantibodies: Anti-Jo1, Anti-PL7, Anti-PL12.
Skin
Alopecia Areata Moderate, A 704.01 Autoantibodies: T-cells.
Synonyms: Alopecia areata - Patchy, Totalis, Universalis
Autoimmune Angioedema Limited, F, N 277.6 995.1
Autoimmune progesterone dermatitis Limited, X, A 279.49
Autoimmune urticaria Comorbidity, A 708
Bullous pemphigoid Moderate, Y 694.5 Autoantibodies: IgG autoantibodies targeting the type XVII collagen component of hemidesmosomes.
Cicatricial pemphigoid Limited, R, X, Y 694.61 precipitates C3.
Autoantibodies: anti-BP-1, anti-BP-2.
Synonyms: Benign Mucosal Pemphigoid, Ocular cicatricial pemphigoid
Dermatitis herpetiformis Moderate, C, Y 694.0 Autoantibodies: IgA Eosinophilia; anti-epidermal transglutaminase antibodies.
Discoid lupus erythematosus Limited, Y III 695.4 IL-2 and IFN-gamma.
Epidermolysis bullosa acquisita Moderate, Y 694.8 COL7A1.
Erythema nodosum Limited, F, Y 695.2
Gestational pemphigoid Limited, R, Y 646.8 Autoantibodies: IgG and C3 misdirected antibodies intended to protect the placenta.
Hidradenitis suppurativa Limited, C, S 705.83
Lichen planus Limited, Y 697.0
Lichen sclerosus Limited, C, Y 701.0
Linear IgA disease (LAD) Moderate, Y 646.8
Morphea Limited, C, S 701.0
Pemphigus vulgaris Moderate, M, A II 694.4 Autoantibodies: Anti-Desmoglein 3 eosinophilia.
Pityriasis lichenoides et varioliformis acuta Limited, C 696.2
Mucha–Habermann disease Limited, C, Y 696.2 T-cells.
Synonyms: Pityriasis lichenoides, varioliformis acuta
Psoriasis Moderate, A IV? 696 CD-8 T-cells, HLA-Cw6, IL-12b, IL-23b, TNFalpha, NF-κB.
Systemic scleroderma Limited, R, S 710.1 COL1A2 and TGF-β1.
Autoantibodies: Anti-nuclear antibodies, anti-centromere and anti-scl70/anti-topoisomerase antibodies.
Synonyms: Diffuse cutaneous systemic sclerosis, Systemic sclerosis, Scleroderma
Vitiligo Limited, C, S 709.01 NALP-1 RERE, PTPN22, LPP, IL2RA, GZMB, UBASH3A and C1QTNF6.

Glands

Organ/Tissue type

Disease name

Level of acceptance for autoimmunity Hypersensitivity

(I,II,III,IV)

ICD-9

Codes

Notes/Autoantibodies/Synonyms/Rare variants
Endocrine
Adrenal gland
Addison's disease Moderate, F, Y 255 Autoantibodies: 21 hydroxylase.
Multi-glandular
Autoimmune polyendocrine syndrome (APS) type 1 Moderate, A Unknown or multiple 258.1 Synonyms: Whitaker's Syndrome, Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), Addisons Disease, Polyglandular Autoimmune Syndrome 1 (PGAS-1).
Autoimmune polyendocrine syndrome (APS) type 2 Moderate, A 258.1 DQ2, DQ8 and DRB1*0404.
Autoantibodies: anti-21 hydroxylase, anti-17 hydroxylase.
Synonyms: Schmidt syndrome, Polyglandular Autoimmune Syndrome 2 (PGAS-2).
Autoimmune polyendocrine syndrome (APS) type 3 Moderate, A 258.1 Synonym: Polyglandular Autoimmune Syndrome 3 (PGAS-3).
Pancreas
Autoimmune pancreatitis (AIP) Moderate, A 577.1 Autoantibodies: ANA, anti-lactoferrin antibodies, anti-carbonic anhydrase antibodies, rheumatoid factor.
Diabetes mellitus type 1 Moderate, A IV 250.01 HLA-DR3, HLA-DR4.
Autoantibodies: Glutamic acid decarboxylase antibodies (GADA), islet cell antibodies (ICA), insulinoma-associated autoantibodies (IA-2), anti-insulin antibodies.
Thyroid gland
Autoimmune thyroiditis Strong, A IV 245.8 HLADR5, CTLA-4.
Autoantibodies: Antibodies against thyroid peroxidase and/or thyroglobulin.
Synonyms: Chronic lymphocytic thyroiditis, Hashimoto's thyroiditis.
Ord's thyroiditis Moderate, Y 245.8
Graves' disease Moderate, M, A II 242.0 Autoantibodies: Thyroid autoantibodies (TSHR-Ab) that activate the TSH-receptor (TSHR).
Exocrine
Reproductive organs
Autoimmune oophoritis Moderate, N 614.2
Endometriosis Limited, S 617.0
Autoimmune orchitis Limited, N 604.0
Salivary glands
Sjögren syndrome Moderate, A 710.2 Autoantibodies: Anti-Ro (often present also in Systemic Lupus Erythematosus).

Digestive system

Organ/Tissue Type

Disease Name

Level of Acceptance for Autoimmunity Hypersensitivity

(I,II,III,IV)

ICD-9

Codes

Notes/Autoantibodies/Synonyms/Rare Variants
Digestive System
Autoimmune enteropathy Moderate, X, Y
Coeliac disease Moderate, A,E IV?? 579.0 HLA-DQ8 and DQ2.5.
Autoantibodies: Anti-tissue transglutaminase antibodies, anti-endomysial IgA, anti-gliadin IgA.
Crohn's disease Moderate, Y IV 555 Innate immunity; Th17; Th1; ATG16L1; CARD15; XBP1.
Esophageal achalasia -Limited, X
Microscopic colitis Limited, S 558.9
Ulcerative colitis Limited, A IV 556

Tissue

Organ/Tissue type

Disease name

Level of acceptance for autoimmunity Hypersensitivity

(I,II,III,IV)

ICD-9

Codes

Notes/Autoantibodies/Synonyms/Rare variants
Blood
Antiphospholipid syndrome (APS, APLS) Moderate, M, A 289.81 HLA-DR7, HLA-B8, HLA-DR2, HLA-DR3.
Autoantibodies: Anti-cardiolipin; anti-pyruvate dehydrogenase; β2 glycoprotein I; phosphatidylserine; anti-apoH; Annexin A5.
Synonym: Hughes syndrome.
Aplastic anemia Limited, F, Y 284
Autoimmune hemolytic anemia Moderate, M, A II 283.0 Complement activation.
Autoimmune lymphoproliferative syndrome Moderate, A 279.41 TNFRSF6; defective Fas-CD95 apoptosis.
Synonym: Canale-Smith syndrome.
Autoimmune neutropenia Moderate, F, N 288.09
Autoimmune thrombocytopenic purpura Moderate, M, R, A 287.31 Autoantibodies: Anti gpIIb-IIIa or 1b-IX.
Synonym: Idiopathic Thrombocytopenic Purpura (ITP)
Cold agglutinin disease Moderate, M, A II 283.0 Idiopathic or secondary to leukemia or infection.
Autoantibodies: IgM.
Synonym: Autoimmune hemolytic anemia.
Essential mixed cryoglobulinemia Limited, C, Y 273.2
Evans syndrome Moderate, Y 287.32 Syndrome with a combination of hemolytic anemia and thrombocytopenic purpura
Pernicious anemia Moderate, A II 281.0 Autoantibodies: Anti-parietal cell antibody.
Pure red cell aplasia Limited, Y 284.81
Thrombocytopenia Limited, F, Y II 287.5 Multiple mechanisms.
Autoantibodies: Glycoproteins IIb-IIIa or Ib-IX in ITP anti-ADAMTS13 in TTP. and HUS anti-cardiolipin (anti-cardiolipin antibodies) and β2 glycoprotein I in Antiphospholipid syndrome; anti-HPA-1a, anti-HPA-5b, and others in NAIT.
Synonyms: Neonatal thrombocytopenia
Connective tissue, systemic, and multi-organ
Adiposis dolorosa Limited, L, S 272.8 Lipoid tissue.
Synonym: Dercum's disease
Adult-onset Still's disease Moderate, Y 714.2 Macrophage migration inhibitory factor.
Autoantibodies: ANA.
Ankylosing spondylitis Limited, S 720.0 CD8; HLA-B27.
CREST syndrome Limited, Y 710.1 Autoantibodies: Anti-centromere antibodies Anti-nuclear antibodies.
Drug-induced lupus Moderate, Y 710.0 Autoantibodies: Anti-histone antibodies.
Enthesitis-related arthritis Limited, C, Y MMP3, TRLR2, TLR4, ERAP1.
A subtype of Juvenile Rheumatoid Arthritis.
Eosinophilic fasciitis Limited, F, A 728.89 Synonym: Shulman's syndrome
Felty syndrome Strong, M, Y 714.1
IgG4-related disease Limited, C, N Characteristic histological features (storiform fibrosis, lymphoplasmacytic infiltrate, obliterative phlebitis) are required for definitive diagnosis.
Synonyms: IgG4-related systemic disease, IgG4-related sclerosing disease, IgG4-related systemic sclerosing disease, IgG4-related autoimmune disease, IgG4-associated multifocal systemic fibrosis, IgG4-associated disease, IgG4 syndrome, Hyper-IgG4 disease, Systemic IgG4-related plasmacytic syndrome.
Juvenile arthritis Strong, M, R, Y 714.30 Autoantibodies: inconsistent ANA, Rheumatoid factor.
Synonyms: Juvenile rheumatoid arthritis, Juvenile idiopathic arthritis
Lyme disease (chronic) Limited, L, T, N 088.81
Mixed connective tissue disease (MCTD) Moderate, M, A 710.8 HLA-DR4.
Autoantibodies: Anti-nuclear antibody, anti-U1-RNP.
Palindromic rheumatism Limited, Y 719.3 Autoantibodies: Anti-cyclic citrullinated peptide antibodies (anti-CCP) and antikeratin antibodies (AKA).
Synonym: Hench-Rosenberg syndrome.
Parry–Romberg syndrome Limited, Y 349.89351.8 Autoantibodies: ANA.
Parsonage–Turner syndrome Limited, Y 353.5
Psoriatic arthritis Moderate, C, A IV? 696.0 HLA-B27.
Reactive arthritis Limited, C, F, Y 099.3
Relapsing polychondritis Strong, A 733.99 Synonyms: Atrophic polychondritis, systemic chondromalacia, chronic atrophic polychondritis, Meyenburg-Altherr-Uehlinger syndrome, generalized chondromalacia, systemic chondromalacia
Retroperitoneal fibrosis Limited, Y 593.4
Rheumatic fever Moderate, T, A II 390 Autoantibodies: Streptococcal M protein cross reacts with human myosin.
Rheumatoid arthritis Strong, M, A III 714 HLA-DR4, PTPN22, depleted B cells, TNF alpha, IL-17, (also maybe IL-1, 6, and 15).
Autoantibodies: Rheumatoid factor (anti-IgGFc), Anti-MCV, ACPAs(Vimentin).
Sarcoidosis Limited, S IV 135 BTNL2; HLA-B7-DR15; HLA DR3-DQ2.
Schnitzler syndrome Limited, L, X, Y 273.1 IgM.
Systemic lupus erythematosus (SLE) Strong, M, A III 695.4 Autoantibodies: Anti-nuclear antibodies, anti-Ro (often present also in Sjögren syndrome). Eosinophilia.
Synonym: Lupus
Undifferentiated connective tissue disease (UCTD) Moderate, C, A 710.9 HLA-DR4.
Autoantibodies: anti-nuclear antibody.
Synonyms: Latent lupus, incomplete lupus
Muscle
Dermatomyositis Moderate, F, X, A 710.3 B- and T-cell perivascular inflammatory infiltrate on muscle biopsy.
Autoantibodies: histidine-tRNA anti-signal recognition peptide Anti-Mi-2 Anti-Jo1.
Synonym: Juvenile dermatomyositis
Fibromyalgia Limited, C, F, N 729.1
Inclusion body myositis Limited, F, Y 359.71 Similar to polymyositis, but does not respond to steroid therapy-activated T8 cells.
Myositis Limited, F, Y 729.1
Myasthenia gravis Strong, M, A II 358 HA-B8 HLA-DR3 HLA-DR1.
Autoantibodies: Nicotinic acetylcholine receptor MuSK protein.
Neuromyotonia Limited, F, S II? 333.90 Autoantibodies: Voltage-gated potassium channels.
Synonym: Isaacs' syndrome
Paraneoplastic cerebellar degeneration Limited, Y IV? II? 334.9 Autoantibodies: anti-Yo (anti-cdr-2 in purkinje fibers) anti-Hu, anti-Tr, antiglutamate receptor.
Polymyositis Limited, F, A 710.4 Autoantibodies: IFN-gamma, IL-1, TNF-alpha, Anti-Jo1, Anti-SRP.
Nervous system
Acute disseminated encephalomyelitis (ADEM) Strong, M, T, A 323.61323.81 Synonyms: Perivenous encephalomyelitis, Acute hemorrhagic leukoencephalitis (AHL, AHLE), Acute necrotizing encephalopathy (ANE), Acute hemorrhagic encephalomyelitis (AHEM), Acute necrotizing hemorrhagic leukoencephalitis (ANHLE), Weston-Hurst syndrome, Hurst's disease.
Acute motor axonal neuropathy Limited, N 356.8
Anti-N-Methyl-D-Aspartate (Anti-NMDA) Receptor Encephalitis Moderate, N
Balo concentric sclerosis Moderate, Y 341.1 Synonyms: Balo disease, Schilders disease.
Bickerstaff's encephalitis Limited, Y 323.62 Similar to Guillain–Barré syndrome.
Autoantibodies: Anti-GQ1b 2/3 patients.
Chronic inflammatory demyelinating polyneuropathy Moderate, C, Y 357.81 Similar to Guillain–Barré syndrome.
Autoantibodies: Anti-ganglioside antibodies.
Synonyms: Relapsing polyneuropathy (CRP), chronic inflammatory demyelinating polyradiculoneuropathy, Chronic inflammatory demyelinating polyneuritis.
Guillain–Barré syndrome Strong, M, A IV 357.0 Autoantibodies: Anti-ganglioside, anti-GQ1b.
Synonyms: Miller–Fisher syndrome, Landry's paralysis.
Hashimoto's encephalopathy Moderate, C, X, A IV Autoantibodies: Alpha-enolase.
Synonyms: Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT), Nonvasculitic autoimmune meningoencephalitis (NAIM), Encephalopathy Associated with Autoimmune Thyroid Disease (EAATD).
Idiopathic inflammatory demyelinating diseases Limited, F, Y 356.8 A set of different variants of multiple sclerosis.
Lambert–Eaton myasthenic syndrome Strong, M, Y 358.1 HLA-DR3-B8.
Autoantibodies: Voltage-gated calcium channels; Q-type calcium channel, synaptogagmin, muscarinic acetylcholine receptor M1.
Multiple sclerosis, pattern II Strong, M, A IV 340 Autoantibody against potassium channel has been reported to present demyelination pattern II. Other cases present autoimmunity against MOG and Anoctamin-2. The three reported autoimmune variants belong to MS pattern II. Also involved HLA-DR2, PECAM-1, Anti-myelin basic protein. Autoantibodies: Anti-Kir4.1, Anti-MOG, Anti-ANO2 (heterogeneous).
Synonyms: Primary progressive multiple sclerosis, Relapsing-remitting multiple sclerosis, disseminated sclerosis, encephalomyelitis disseminata. Also interesting is Multiple sclerosis with HLA-DRB3 histocompatibility. In this case the auto-antigen has been found and is GDP-L-fucose synthase
Oshtoran syndrome X F06.9 Heritable, abnormalities in the kynurenine and glutamate metabolism.
Progressive inflammatory neuropathy Limited, X, S 356.4 Similar to Guillain–Barré syndrome.
Autoantibodies: Anti-ganglioside antibodies:anti-GM1, anti-GD1a, anti-GQ1b.
Restless legs syndrome Limited, C, S 333.94 May occur in Sjögren syndrome, coeliac disease and rheumatoid arthritis, or in derangements of iron metabolism.
Stiff-person syndrome Limited, S 333.91 GLRA1 (glycine receptor).
Autoantibodies: Glutamic acid decarboxylase (GAD).
Sydenham's chorea Limited, T, Y 392
Transverse myelitis Limited, M, A 323.82341.2
Eyes
Autoimmune retinopathy Limited, X, N
Autoimmune uveitis Moderate, F, A 364 Autoantibodies: HLAB-27.
Cogan syndrome Limited, F, Y 370.52
Graves' ophthalmopathy Moderate, M, N 242.9
Intermediate uveitis Limited, L, Y 364.3 Synonyms: Pars planitis, peripheral uveitis.
Ligneous conjunctivitis Limited, L, N 372.39
Mooren's ulcer Limited, L, N 370.07
Neuromyelitis optica Limited, M, Y II? 341.0 Autoantibodies: NMO-IgG aquaporin 4.
Synonym: Devic's disease.
Opsoclonus myoclonus syndrome Limited, X, S IV? 379.59 Lymphocyte recruitment to CSF.
Optic neuritis Limited, C, Y 377.30
Scleritis Limited, C, Y 379.0
Susac's syndrome Limited, C, Y 348.39 Synonym: Retinocochleocerebral vasculopathy.
Sympathetic ophthalmia Limited, I, Y 360.11 Autoantibodies: ocular antigens following trauma.
Tolosa–Hunt syndrome Limited, I, X, Y 378.55
Ears
Autoimmune inner ear disease (AIED) Limited, A 388.8
Ménière's disease Limited, Y III? 386.00 Autoantibodies: Major peripheral myelin protein P0.
Vascular system
Behçet's disease Limited, I, X, A 136.1 An immune-mediated systemic vasculitis; linkage to HLA-B51 (HLA-B27); very variable manifestations, with ulcers as common symptom.
Synonyms: Morbus Adamandiades-Behçet.
Rare variant: Hughes–Stovin syndrome.
Eosinophilic granulomatosis with polyangiitis (EGPA) Limited, I, X, Y 446.4 Autoantibodies: p-ANCA Eosinophilia.
Giant cell arteritis Limited, I, R, A IV 446.5 Synonyms: Cranial arteritis, temporal arteritis.
Granulomatosis with polyangiitis (GPA) Strong, M, A 446.4 Autoantibodies: Anti-neutrophil cytoplasmic (cANCA).
IgA vasculitis (IgAV) Limited, L, Y 287.0 Autoantibodies: IgA and complement component 3 (C3).
Synonyms: Anaphylactoid purpura, Henoch-Schonlein purpura, purpura rheumatica, Schönlein–Henoch purpura.
Kawasaki disease Moderate, S,E 446.1 ITPKC HLA-B51.
Synonyms: Kawasaki syndrome, lymph node syndrome, mucocutaneous lymph node syndrome.
Leukocytoclastic vasculitis Limited, L, Y 447.6
Lupus vasculitis Moderate, C, N 583.81 A comorbidity of systemic lupus erythematosus.
Rheumatoid vasculitis Moderate, C, N 447.6 A symptom of lupus.
Microscopic polyangiitis (MPA) Limited, Y 446.0 Binds to neutrophils causing them to degranulate and damages endothelium.
Autoantibodies: p-ANCA myeloperoxidase.
Synonyms: Microscopic polyarteritis, microscopic polyarteritis nodosa.
Polyarteritis nodosa (PAN) Limited, L, Y 446.0 Synonyms: Panarteritis nodosa, periarteritis nodosa, Kussmaul disease, Kussmaul–Maier disease.
Polymyalgia rheumatica Limited, L, Y 725
Urticarial vasculitis Limited, X, Y II? 708.9 Clinically may resemble type I hypersensitivity.
Autoantibodies: anti C1q antibodies.
Vasculitis Strong, I, M, F, A III 447.6 Autoantibodies: ANCA (sometimes).
Systemic
Primary immunodeficiency Limited, N

Autoimmune comorbidities

This list includes conditions that are not diseases but signs common to autoimmune disease. Some, such as chronic fatigue syndrome, are controversial. These conditions are included here because they are frequently listed as autoimmune diseases but should not be included in the list above until there is more consistent evidence.

Organ/Tissue Type

Disease Name

Level of Acceptance for Autoimmunity Hypersensitivity

(I,II,III,IV)

ICD-9

Codes

Notes/Autoantibodies/Synonyms
Chronic fatigue syndrome Comorbidity, N Symptomatic of autoimmune diseases or autoimmune activity, but not a disease or a cause of disease.
Complex regional pain syndrome Comorbidity, N Symptomatic of autoimmune diseases or autoimmune activity, but not a disease or a cause of disease. Synonyms: Amplified Musculoskeletal Pain Syndrome, Reflex Neurovascular Dystrophy, Reflex sympathetic dystrophy
Eosinophilic esophagitis Comorbidity, N 530.13
Gastritis Comorbidity, Y Possibly symptomatic of autoimmune diseases, but not a disease or a cause of disease. Autoantibodies: serum antiparietal and anti-IF antibodies.
Interstitial lung disease Comorbidity, N Associated with several autoimmune connective tissue diseases.
POEMS syndrome Comorbidity, Y Possibly symptomatic of autoimmune diseases, but not a disease or a cause of disease. Autoantibodies: interleukin 1β, interleukin 6 and TNFα. vascular endothelial growth factor (VEGF), given the ..
Raynaud's phenomenon Comorbidity, S Symptomatic of autoimmune diseases or autoimmune activity, but not a disease or a cause of disease.
Primary immunodeficiency Comorbidity, N 279.8 The condition is inherited, but it is associated with several autoimmune diseases.
Pyoderma gangrenosum Comorbidity, Y Possibly symptomatic of autoimmune diseases, but not a disease or a cause of disease.

Non-autoimmune

At this time, there is not sufficient evidence—direct, indirect, or circumstantial—to indicate that these diseases are caused by autoimmunity. These conditions are included here because:

  1. The disease was listed in the prior version of this table
  2. The disease is included in several widely used lists of autoimmune disease and is shown here to ensure that a person visiting this page does not conclude that the disease was not considered. Before moving a condition from here to the list of autoimmune diseases, references should be provided in the Wikipedia page for the condition that point to evidence, direct or indirect, that it is an autoimmune disease.
Organ/Tissue Type

Disease Name

Level of Acceptance for Autoimmunity Hypersensitivity

(I,II,III,IV)

ICD-9

Codes

Notes/Autoantibodies/Synonyms
Agammaglobulinemia Not Autoimmune, Y 279.00 An immune system disorder but not an autoimmune disease.. Autoantibodies: IGHM; IGLL1: CD79A; CD79B; BLNK; LRRC8A.
Amyloidosis Not Autoimmune, N 277.30 No consistent evidence of association with autoimmunity.
Amyotrophic lateral sclerosis Not Autoimmune, Y 335.20 No consistent evidence of association with autoimmunity. Autoantibodies: Amyotrophic lateral sclerosis (Also Lou Gehrig's disease; Motor Neuron Disease).
Anti-tubular basement membrane nephritis Not Autoimmune, N No consistent evidence of association with autoimmunity.
Atopic allergy Not Autoimmune, Y I 691.8 A hypersensitivity.
Atopic dermatitis Not Autoimmune, Y I 691.8 A hypersensitivity.
Autism Not Autoimmune, N No consistent evidence of association with maternal autoimmunity.
Autoimmune peripheral neuropathy Not Autoimmune, F, A A symptom of many diseases, including some that may be autoimmune. Not an autoimmune disease.
Blau syndrome Not Autoimmune, Y Overlaps both sarcoidosis and granuloma annulare. No evidence of association with autoimmunity.
Cancer Not Autoimmune, Y No consistent evidence of association with autoimmunity.
Castleman's disease Not Autoimmune, Y An immune system disorder but not an autoimmune disease.. Autoantibodies: Over expression of IL-6.
Chagas disease Not Autoimmune, S No consistent evidence of association with autoimmunity.
Chronic obstructive pulmonary disease Not Autoimmune, S No consistent evidence of association with autoimmunity.
Chronic recurrent multifocal osteomyelitis Not Autoimmune, Y LPIN2, D18S60. Synonyms: Majeed syndrome
Complement component 2 deficiency Not Autoimmune, Y Possibly symptomatic of autoimmune diseases, but not a disease.
Congenital heart block Not Autoimmune, N May be related to autoimmune activity in the mother.
Contact dermatitis Not Autoimmune, Y IV A hypersensitivity.
Cushing's syndrome Not Autoimmune, Y No consistent evidence of association with autoimmunity.
Cutaneous leukocytoclastic angiitis Not Autoimmune, Y No consistent evidence of association with autoimmunity. Autoantibodies: neutrophils.
Dego's disease Not Autoimmune, Y No consistent evidence of association with autoimmunity.
Eczema Autoimmune, Y eczema is an autoimmune disease. It was previously thought not to be, but has been accepted as an autoimmune disease since at least 2014. Eczema and Psoriasis are both autoimmune diseases.
Eosinophilic gastroenteritis Not Autoimmune, Y Possibly a hypersensitivity. Autoantibodies: IgE, IL-3, IL-5, GM-CSF, eotaxin.
Eosinophilic pneumonia Not Autoimmune, F, Y A class of diseases, some of which may be autoimmune. Specifically, Churg–Strauss syndrome, a subtype of Eosinophilic pneumonia, is autoimmune.
Erythroblastosis fetalis Not Autoimmune, Y II Mother's immune system attacks fetus. An immune system disorder but not autoimmune. Autoantibodies: ABO, Rh, Kell antibodies.
Fibrodysplasia ossificans progressiva Not Autoimmune, Y Possibly an immune system disorder but not autoimmune. Autoantibodies: ACVR1 Lymphocytes express increased BMP4.
Gastrointestinal pemphigoid Not Autoimmune, A No consistent evidence of association with autoimmunity.
Hypogammaglobulinemia Not Autoimmune, Y An immune system disorder but not autoimmune. Autoantibodies: IGHM, IGLL1, CD79A, BLNK, LRRC8A, CD79B.
Idiopathic giant-cell myocarditis Not Autoimmune, N No consistent evidence of autoimmune cause though the disease has been found comorbid with other autoimmune diseases. Synonyms: Giant cell myocarditis
Idiopathic pulmonary fibrosis Not Autoimmune, Y Autoantibodies: SFTPA1, SFTPA2, TERT, and TERC.. Synonyms: Fibrosing alveolitis
IgA nephropathy Not Autoimmune, Y III? Autoantibodies: IgA produced from marrow rather than MALT. Synonyms: IgA nephrits, Berger's disease, Synpharyngitic Glomerulonephritis. An immune system disorder but not an autoimmune disease.
Immunoregulatory lipoproteins Not Autoimmune, N Not a disease.
IPEX syndrome Not Autoimmune, N A genetic mutation in FOXP3 that leads to autoimmune diseases, but no consistent evidence that it is an autoimmune disorder itself.. Synonyms: X-linked polyendocrinopathy, immunodeficiency and diarrhea-syndrome (XLAAD)
Ligneous conjunctivitis Not Autoimmune, N No consistent evidence of association with autoimmunity.
Majeed syndrome Not Autoimmune, Y No consistent evidence of association with autoimmunity. Autoantibodies: LPIN2.
Narcolepsy Not Autoimmune, Y II? No evidence of association with autoimmunity. Research not reproducible. Autoantibodies: hypocretin or orexin, HLA-DQB1*0602.
Rasmussen's encephalitis Not Autoimmune, Y No consistent evidence of association with autoimmunity. Autoantibodies: anti-NR2A antibodies.
Schizophrenia Not Autoimmune, S No consistent evidence of association with autoimmunity.
Serum sickness Not Autoimmune, Y III A hypersensitivity.
Spondyloarthropathy Not Autoimmune, Y No consistent evidence of association with autoimmunity. Autoantibodies: HLA-B27.
Sweet's syndrome Not Autoimmune, Y No consistent evidence of association with autoimmunity. Autoantibodies: GCSF.
Takayasu's arteritis Not Autoimmune, Y No consistent evidence of association with autoimmunity.
Undifferentiated spondyloarthropathy Not Autoimmune, Y See Enthesitis-related arthritis.

See also


Новое сообщение