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Hypersensitivity
Wikipedia
Testing can be done via skin test for specific IgE. [2] Atopy Anaphylaxis Asthma Churg-Strauss Syndrome II Cytotoxic , Antibody-dependent Antibody IgM Antibody IgG Complement MAC Antibody (IgM or IgG) binds to antigen on a target cell, which is actually a host cell that is perceived by the immune system as foreign, leading to cellular destruction via the MAC . Testing includes both the direct and indirect Coombs test . [3] Autoimmune hemolytic anemia Rheumatic heart disease Thrombocytopenia Erythroblastosis fetalis Goodpasture's syndrome Graves' disease [note 1] Myasthenia gravis [note 1] III Immune complex Antibody IgG Complement Neutrophils Antibody (IgG) binds to soluble antigen, forming a circulating immune complex . ... External links [ edit ] Classification D ICD - 10 : T78.4 ICD - 9-CM : 995.3 MeSH : D006967 DiseasesDB : 28827 v t e Consequences of external causes Temperature Elevated Hyperthermia Heat syncope Reduced Hypothermia Immersion foot syndromes Trench foot Tropical immersion foot Warm water immersion foot Chilblains Frostbite Aerosol burn Cold intolerance Acrocyanosis Erythrocyanosis crurum Radiation Radiation poisoning Radiation burn Chronic radiation keratosis Eosinophilic, polymorphic, and pruritic eruption associated with radiotherapy Radiation acne Radiation-induced cancer Radiation recall reaction Radiation-induced erythema multiforme Radiation-induced hypertrophic scar Radiation-induced keloid Radiation-induced morphea Air Hypoxia / Asphyxia Barotrauma Aerosinusitis Decompression sickness High altitude Altitude sickness Chronic mountain sickness Death zone HAPE HACE Food Starvation Maltreatment Physical abuse Sexual abuse Psychological abuse Travel Motion sickness Seasickness Airsickness Space adaptation syndrome Adverse effect Hypersensitivity Anaphylaxis Angioedema Allergy Arthus reaction Adverse drug reaction Other Electrical injury Drowning Lightning injuries Ungrouped skin conditions resulting from physical factors Dermatosis neglecta Pinch mark Pseudoverrucous papules and nodules Sclerosing lymphangitis Tropical anhidrotic asthenia UV-sensitive syndrome environmental skin conditions Electrical burn frictional/traumatic/sports Black heel and palm Equestrian perniosis Jogger's nipple Pulling boat hands Runner's rump Surfer's knots Tennis toe Vibration white finger Weathering nodule of ear Wrestler's ear Coral cut Painful fat herniation Uranium dermatosis iv use Skin pop scar Skin track Slap mark Pseudoacanthosis nigricans Narcotic dermopathy v t e Lymphoid and complement disorders causing immunodeficiency Primary Antibody / humoral ( B ) Hypogammaglobulinemia X-linked agammaglobulinemia Transient hypogammaglobulinemia of infancy Dysgammaglobulinemia IgA deficiency IgG deficiency IgM deficiency Hyper IgM syndrome ( 1 2 3 4 5 ) Wiskott–Aldrich syndrome Hyper-IgE syndrome Other Common variable immunodeficiency ICF syndrome T cell deficiency ( T ) thymic hypoplasia : hypoparathyroid ( Di George's syndrome ) euparathyroid ( Nezelof syndrome Ataxia–telangiectasia ) peripheral: Purine nucleoside phosphorylase deficiency Hyper IgM syndrome ( 1 ) Severe combined (B+T) x-linked: X-SCID autosomal: Adenosine deaminase deficiency Omenn syndrome ZAP70 deficiency Bare lymphocyte syndrome Acquired HIV/AIDS Leukopenia : Lymphocytopenia Idiopathic CD4+ lymphocytopenia Complement deficiency C1-inhibitor ( Angioedema / Hereditary angioedema ) Complement 2 deficiency / Complement 4 deficiency MBL deficiency Properdin deficiency Complement 3 deficiency Terminal complement pathway deficiency Paroxysmal nocturnal hemoglobinuria Complement receptor deficiency v t e Hypersensitivity and autoimmune diseases Type I / allergy / atopy ( IgE ) Foreign Atopic eczema Allergic urticaria Allergic rhinitis (Hay fever) Allergic asthma Anaphylaxis Food allergy common allergies include: Milk Egg Peanut Tree nut Seafood Soy Wheat Penicillin allergy Autoimmune Eosinophilic esophagitis Type II / ADCC IgM IgG Foreign Hemolytic disease of the newborn Autoimmune Cytotoxic Autoimmune hemolytic anemia Immune thrombocytopenic purpura Bullous pemphigoid Pemphigus vulgaris Rheumatic fever Goodpasture syndrome Guillain–Barré syndrome " Type V "/ receptor Graves' disease Myasthenia gravis Pernicious anemia Type III ( Immune complex ) Foreign Henoch–Schönlein purpura Hypersensitivity vasculitis Reactive arthritis Farmer's lung Post-streptococcal glomerulonephritis Serum sickness Arthus reaction Autoimmune Systemic lupus erythematosus Subacute bacterial endocarditis Rheumatoid arthritis Type IV / cell-mediated ( T cells ) Foreign Allergic contact dermatitis Mantoux test Autoimmune Diabetes mellitus type 1 Hashimoto's thyroiditis Multiple sclerosis Coeliac disease Giant-cell arteritis Postorgasmic illness syndrome Reactive arthritis GVHD Transfusion-associated graft versus host disease Unknown/ multiple Foreign Hypersensitivity pneumonitis Allergic bronchopulmonary aspergillosis Transplant rejection Latex allergy (I+IV) Autoimmune Sjögren syndrome Autoimmune hepatitis Autoimmune polyendocrine syndrome APS1 APS2 Autoimmune adrenalitis Systemic autoimmune disease Biology portal Medicine portalCCL2, HLA-B, IL17A, IL4, PPBP, CCL8, CCL7, CCL4, CCL3, MAP2K6, PF4, IL16, MYLK, MTHFR, CXCL9, KNG1, ITGB2, IL18, CCL11, ABCF1, CCL19, CCL20, COMMD1, CLEC4A, CD274, CCR9, IL1R2, TNFRSF1B, TNFRSF1A, TNF, TGFB1, TAC1, SPP1, SELP, CX3CL1, CXCL5, CCL24, CCL17, CCR2, IL13, HLA-DRB4, ALB, CASP1, CD40LG, CCR1, CCR6, CSF2RA, CXCR2, DSG1, CXCR3, CXCL1, HLA-DQA1, HLA-DQB1, HLA-DRB1, CYP1A1, HLA-DRB5, IL2RB, IL6, IL6ST, IFNG, IL5RA, HP, IL1B, IL1R1, AKR1B1, CHD1, BBS1, ADA, ARID1B, FOXP3, CSTA, CCDC28B, MTOR, TGM5, TRPA1, HAVCR2, IL31, TLR4, CD14, TRPV1, JAK2, TLR2, CRHR1, SLC6A3, SFTPD, F2RL1, NOS1, GZMB, HTR2B, LMAN1
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Hypospadias-Intellectual Disability, Goldblatt Type Syndrome
Orphanet
Hypospasdias – intellectual deficit, Goldblatt type is a very rare multiple congenital anomalies syndrome described in three brothers of one South-African family, and characterized by hypospadias and intellectual deficit, in association with mirocephaly, craniofacial dysmorphism, joint laxity and beaked nails.
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Siegler-Brewer-Carey Syndrome
Orphanet
A rare, syndromic, genetic respiratory disease characterized by cataracts, otitis media, intestinal malabsorption, chronic respiratory infections, and failure to thrive.
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Pili Torti-Onychodysplasia Syndrome
Orphanet
A rare ectodermal dysplasia syndrome characterized by congenital onychodystrophy (particularly of the distal nail) and severe hypotrichosis with alopecia involving the eyebrows, eyelashes and body hair.
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X-Linked Intellectual Disability-Plagiocephaly Syndrome
Orphanet
A rare, syndromic intellectual disability characterized by severe intellectual deficit, brachycephaly, plagiocephaly, and prominent forehead in male patients.
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Trigonocephaly-Broad Thumbs Syndrome
Orphanet
Trigonocephaly-broad thumbs syndrome is characterized by neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers 1, 2, and 5, and broad toes with duplication of the terminal phalanx.
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Microbrachycephaly-Ptosis-Cleft Lip Syndrome
Orphanet
Microbrachycephaly-ptosis-cleft lip syndrome is characterised by the association of intellectual deficit, microbrachycephaly, hypotelorism, palpebral ptosis, a thin/long face, cleft lip, and anomalies of the lumbar vertebra, sacrum and pelvis.
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Non-Eruption Of Teeth-Maxillary Hypoplasia-Genu Valgum Syndrome
Orphanet
Noneruption of teeth - maxillary hypoplasia - genu valgum is an extremely rare syndrome that is characterized by multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears.
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O'sullivan-Mcleod Syndrome
Orphanet
O' Sullivan McLeod syndrome is a benign lower motor neuron disorder and a rare variant of monomelic amyotrophy (MA; see this term), characterized by an initial unilateral weakness in the intrinsic hand muscles that eventually spreads to the opposite limb (with an asymmetrical distribution) and that has a very slow progression of muscular atrophy over a 20 year period.
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Osteogenesis Imperfecta-Retinopathy-Seizures-Intellectual Disability Syndrome
Orphanet
Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome is characterized by osteogenesis imperfecta, wormian bones, optic atrophy, retinopathy, seizures and severe developmental delay.
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Infantile Choroidocerebral Calcification Syndrome
Orphanet
A rare syndromic intellectual disability characterized by severe intellectual disability and calcification of the choroid plexus, associated with elevated cerebrospinal fluid protein concentration.
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Spinal Atrophy-Ophthalmoplegia-Pyramidal Syndrome
Orphanet
Spinal atrophy-ophthalmoplegia-pyramidal syndrome is a rare, bulbospinal muscular atrophy characterized by generalized neonatal hypotonia, progressive pontobulbar and spinal palsy, pyramidal signs, and deafness.
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Diaphragmatic Hernia-Short Bowel-Asplenia Syndrome
Orphanet
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by congenital diaphragmatic hernia, short bowel, and asplenia.
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Dentin Dysplasia-Sclerotic Bones Syndrome
Orphanet
Dentin dysplasia-sclerotic bones syndrome is a rare, genetic odontologic disease characterized by the clinical, radiographic, and histologic features of dentine dysplasia and osteosclerosis of all long bones, with heavy cortical bone and narrowed or occluded marrow spaces.
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Ectodermal Dysplasia-Sensorineural Deafness Syndrome
Orphanet
Ectodermal dysplasia-sensorineural deafness syndrome is characterised by hidrotic ectodermal dysplasia, sensorineural hearing loss, and contracture of the fifth fingers.
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Early-Onset Parkinsonism-Intellectual Disability Syndrome
Orphanet
A rare X-linked syndromic intellectual disability characterized by infantile-onset non-progressive intellectual deficit (with psychomotor developmental delay, cognitive impairment and macrocephaly) and early-onset parkinsonism (before 45 years of age), in male patients.
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Waterhouse–friderichsen Syndrome
Gard
Waterhouse–Friderichsen syndrome is adrenal gland failure due to bleeding into the adrenal gland.
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Tranebjaerg Svejgaard Syndrome
Gard
Tranebjaerg Svejgaard syndrome is a rare condition that is characterized by intellectual disability, seizures and psoriasis .
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Chronic Epstein-Barr Virus Infection Syndrome
Orphanet
Chronic Epstein-Barr virus infection syndrome is a rare infectious disease characterized by familial, primary, chronic Epstein-Barr virus infection which typically manifests with persistent mononucleosis-like signs and symptoms, in the absence of secondary immunodeficiency.
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Ichthyosis-Intellectual Disability-Dwarfism-Renal Impairment Syndrome
Orphanet
Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome is characterised by nonbullous congenital ichthyosis, intellectual deficit, dwarfism and renal impairment.