List of autoimmune diseases
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 suffer from 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[1][2] | Moderate, F, R, A | 391.2422429.0 | Synonyms: Autoimmune myocarditis, Autoimmune cardiomyopathy, Coxsackie myocarditis | |
Postmyocardial infarction syndrome[2] | 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)[3] | Limited, Y | III | 421.0 | Autoantibodies: essential mixed cryoglobulinemia. |
Kidney | ||||
Anti-Glomerular Basement Membrane nephritis[4] | 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[5] | Limited, S | 595.1 | Mast cells. | |
Liver | ||||
Autoimmune hepatitis[6][7][8] | 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%).[citation needed] Synonym: Lupoid hepatitis |
Primary biliary cholangitis (PBC)[9][10][11][12] | Moderate, A | 571.6 | Autoantibodies: Anti-p62, Anti-sp100, Anti-Mitochondrial(M2), Anti-Ro aka SSA. Note that 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[13][14] | Moderate, A | 704.01 | Autoantibodies: T-cells. Synonyms: Alopecia areata - Patchy, Totalis, Universalis | |
Autoimmune Angioedema[15] | Limited, F, N | 277.6 995.1 | ||
Autoimmune progesterone dermatitis | Limited, X, A | 279.49 | ||
Autoimmune urticaria[16][17] | Comorbidity, A | 708 | ||
Bullous pemphigoid[18] | 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[19] | Moderate, C, Y | 694.0 | Autoantibodies: IgA Eosinophilia; anti-epidermal transglutaminase antibodies. | |
Discoid lupus erythematosus[20] | 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[21] | Limited, C, S | 705.83 | ||
Lichen planus | Limited, Y | 697.0 | ||
Lichen sclerosus | Limited, C, Y | 701.0 | ||
Linear IgA disease (LAD)[22] | Moderate, Y | 646.8 | ||
Morphea[23] | Limited, C, S | 701.0 | ||
Pemphigus vulgaris[4][19] | 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[24] | Moderate, A | IV? | 696 | CD-8 T-cells, HLA-Cw6, IL-12b, IL-23b, TNFalpha, NF-κB. |
Systemic scleroderma[23][25] | 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[26][27] | 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[4] | 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[28] | 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[4] | 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[4] | 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[29] | Limited, S | 617.0 | ||
Autoimmune orchitis | Limited, N | 604.0 | ||
Salivary glands | ||||
Sjögren syndrome[4][10][11][12] | 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[30][31][32] | 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[33] | Moderate, Y | IV | 555 | Innate immunity; Th17; Th1; ATG16L1; CARD15; XBP1. |
Esophageal achalasia | -Limited, X | [34] | ||
Microscopic colitis | Limited, S | 558.9 | ||
Ulcerative colitis[4] | 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)[4] | 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[4] | 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[35] | Moderate, A | II | 281.0 | Autoantibodies: Anti-parietal cell antibody. |
Pure red cell aplasia | Limited, Y | 284.81 | ||
Thrombocytopenia[36][37] | 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[38] | Limited, L, S | 272.8 | Lipoid tissue. Synonym: Dercum's disease | |
Adult-onset Still's disease[39] | Moderate, Y | 714.2 | Macrophage migration inhibitory factor. Autoantibodies: ANA. | |
Ankylosing spondylitis[15] | 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[40][41][42][43] | 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[44] | 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[39] | Strong, M, R, Y | 714.30 | Autoantibodies: inconsistent ANA, Rheumatoid factor. Synonyms: Juvenile rheumatoid arthritis, Juvenile idiopathic arthritis | |
Lyme disease (chronic)[45] | Limited, L, T, N | 088.81 | ||
Mixed connective tissue disease (MCTD)[4] | Moderate, M, A | 710.8 | HLA-DR4. Autoantibodies: Anti-nuclear antibody, anti-U1-RNP. | |
Palindromic rheumatism[46] | 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[47] | Moderate, C, A | IV? | 696.0 | HLA-B27. |
Reactive arthritis | Limited, C, F, Y | 099.3 | ||
Relapsing polychondritis[48] | 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[49][50] | Moderate, T, A | II | 390 | Autoantibodies: Streptococcal M protein cross reacts with human myosin. |
Rheumatoid arthritis[4] | 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[51][52][53] | Limited, S | IV | 135 | BTNL2; HLA-B7-DR15; HLA DR3-DQ2. |
Schnitzler syndrome | Limited, L, X, Y | 273.1 | IgM. | |
Systemic lupus erythematosus (SLE)[4][10][11][12][19][54] | 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[55][56] | 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[4] | Strong, M, A | II | 358 | HA-B8 HLA-DR3 HLA-DR1. Autoantibodies: Nicotinic acetylcholine receptor MuSK protein. |
Neuromyotonia[57] | Limited, F, S | II? | 333.90 | Autoantibodies: Voltage-gated potassium channels. Synonym: Isaacs' syndrome |
Paraneoplastic cerebellar degeneration[58][59][60] | Limited, Y | IV? II? | 334.9 | Autoantibodies: anti-Yo (anti-cdr-2 in purkinje fibers) anti-Hu, anti-Tr, antiglutamate receptor. |
Polymyositis[55] | 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[61] | Limited, N | 356.8 | ||
Anti-N-Methyl-D-Aspartate (Anti-NMDA) Receptor Encephalitis[62] | 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[63] | 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[4] | Strong, M, A | IV | 357.0 | Autoantibodies: Anti-ganglioside, anti-GQ1b. Synonyms: Miller–Fisher syndrome, Landry's paralysis. |
Hashimoto's encephalopathy[4][64] | 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[65][66] | Strong, M, A | IV | 340 | Autoantibody against potassium channel has been reported to present demyelination pattern II. Other cases present autoimmunity against MOG[67] and Anoctamin-2.[68] 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[69] |
[70] | X | F06.9 | Heritable, abnormalities in the kynurenine and glutamate metabolism. | |
Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcus (PANDAS) | Limited, F, S | II? | 279.49 | Antibodies against streptococcal infection serve as auto-antibodies. |
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[71] | 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[72] | 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[73][74] | Limited, M, Y | II? | 341.0 | Autoantibodies: NMO-IgG aquaporin 4. Synonym: Devic's disease. |
Opsoclonus myoclonus syndrome[75] | 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)[76] | Limited, A | 388.8 | ||
Ménière's disease[77] | 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)[19][78] | Limited, I, X, Y | 446.4 | Autoantibodies: p-ANCA Eosinophilia. | |
Giant cell arteritis[4] | Limited, I, R, A | IV | 446.5 | Synonyms: Cranial arteritis, temporal arteritis. |
Granulomatosis with polyangiitis (GPA)[78] | Strong, M, A | 446.4 | Autoantibodies: Anti-neutrophil cytoplasmic (cANCA). | |
IgA vasculitis (IgAV)[78] | 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[79] | 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[80] | Limited, X, Y | II? | 708.9 | Clinically may resemble type I hypersensitivity. Autoantibodies: anti C1q antibodies. |
Vasculitis[18] | 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.[2] 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[81] | 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[82] | 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:
- The disease was listed in the prior version of this table
- 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). | |
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[83] | Not Autoimmune, S | No consistent evidence of association with autoimmunity. | ||
Chronic obstructive pulmonary disease[84][85] | 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. | ||
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[86] | 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[87] | 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. | |
[88] | 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[89][90][91][92] | 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[93][94][95] | 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. | ||
Not Autoimmune, Y | See . |
See also[]
References[]
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- Autoimmune diseases
- Lists of diseases