Disease

Common Variable Immunodeficiency


About the Disease
Common Variable Immunodeficiency, also known as cvid, is related to immunodeficiency, common variable, 1 and immunodeficiency, common variable, 2. An important gene associated with Common Variable Immunodeficiency is TNFRSF13B (TNF Receptor Superfamily Member 13B), and among its related pathways/superpathways are ERK Signaling and MIF Mediated Glucocorticoid Regulation. The drugs Rifaximin and Budesonide have been mentioned in the context of this disorder. Affiliated tissues include t cells, b cells and lung, and related phenotypes are chronic otitis media and brachycephaly

Common Targets / Biomarkers
G6929 | G5293 | G10320 | G975 | G6899 | G3105 | G987 | G10388 | G4791 | G8741 | G101927840 | G64127 | G5880 | G359948 | G6941 | G105369166 | G3575 | G8742 | G4439 | G8547 | G9726 | G5460 | G1493 | G7015 | G3113 | G23266 | G3118 | G60468 | G10111 | G51750 | G728734 | G66037 | G56259 | G2212 | G3115 | G3119 | G23274 | G2521 | G3107 | G115650 | G55072 | G930 | G6774 | G101929772 | G5896 | G3123 | G4790 | G50943 | G105375005 | G105375013 | G100532732 | G23495 | G3106 | G91662 | G3684 | G338005 | G1380 | G5336 | G29851 | G3117 | G2220

Other Diseases

Communication Disorders | Compartment Syndrome | Conduct Disorder | Cone Dystrophy | Congenital Absence Of Vas Deferens | Congenital Adrenal Hyperplasia | Congenital Adrenal Hyperplasia 1 | Congenital Afibrinogenemia | Congenital Aniridia | Congenital Bilateral Absence Of Vas Deferens | Congenital Bile Acid Synthesis Defect | Congenital Central Hypoventilation Syndrome | Congenital Diaphragmatic Hernia | Congenital Disorders Of Glycosylation | Congenital Disorders Of Glycosylation Type II | Congenital Dyserythropoietic Anemia | Congenital Dyserythropoietic Anemia Type 1 | Congenital Dyserythropoietic Anemia Type 4 | Congenital Dysfibrinogenemia | Congenital Fiber-type Disproportion Myopathy | Congenital Generalized Lipodystrophy | Congenital Heart Block | Congenital Heart Defects | Congenital Hemolytic Anemia | Congenital Hereditary Endothelial Dystrophy Type II | Congenital Hypofibrinogenemia | Congenital Ichthyosiform Erythroderma | Congenital Lipoid Adrenal Hyperplasia | Congenital Mirror Movements | Congenital Muscular Dystrophy | Congenital Myasthenic Syndrome | Congenital Myopathy | Congenital Nephrotic Syndrome | Congenital Nystagmus | Congenital Poikiloderma | Congenital Primary Aphakia | Congenital Sodium Diarrhea | Congenital Stationary Night Blindness | Congenital Stromal Corneal Dystrophy | Congenital Torticollis | Congenital Tufting Enteropathy | Congestive Heart Failure | Conjunctivitis | Conjunctivitis, Allergic | Connective Tissue Disorders | Constipation | Contact Dermatitis | Corneal Dystrophies, Hereditary | Corneal Dystrophy | Corneal Dystrophy And Perceptive Deafness | Corneal Edema | Corneal Neovascularization | Corneal Ulcer | Cornelia De Lange Syndrome | Coronary Artery Disease | Coronary Heart Disease | Coronary Restenosis | Corticobasal Syndrome | Costello Syndrome | Cousin Syndrome | Cramp Fasciculation Syndrome | Cranial Nerve Disease | Cranioectodermal Dysplasia | Craniofacial Dysostosis | Craniofrontonasal Syndrome | Craniolenticulosutural Dysplasia | Craniometaphyseal Dysplasia | Craniopharyngioma | Craniosynostosis | Creatine Deficiency Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | CREST Syndrome | Cri-du-chat Syndrome | Crigler-Najjar Syndrome | Crimean-Congo Hemorrhagic Fever | Cryopyrin-associated Periodic Syndromes | Cryptococcal Meningitis | Cryptorchidism | Cryptosporidiosis | Currarino Syndrome | Cushing Syndrome | Cutaneous Angiosarcoma | Cutaneous Lupus Erythematosus | Cutaneous Mastocytosis | Cutaneous T-cell Lymphoma | Cutis Laxa | Cyclic Vomiting Syndrome | Cyst | Cysticercosis | Cystinosis | Cystinuria | Cystitis | Cystitis, Interstitial | D-2-Hydroxyglutaric Aciduria | Danon Disease | Delayed Sleep Phase Syndrome | Delirium | Dementia | Dementia, Vascular | DEND Syndrome | Dengue Hemorrhagic Fever | Dengue Shock Syndrome | Dent Disease | Dental Caries | Dentinogenesis Imperfecta | Depression | Dermatitis | Dermatitis Herpetiformis | Dermatofibrosarcoma | Dermatomyositis | Desbuquois Syndrome | Desmosterolosis | Diabetes | Diabetes Gestational | Diabetes Insipidus | Diabetes Insipidus, Nephrogenic | Diabetes Insipidus, Neurogenic | Diabetes Mellitus, Transient Neonatal | Diabetes Type 1 | Diabetes Type 2 | Diabetic Encephalopathy | Diabetic Macular Edema | Diabetic Nephropathy | Diabetic Neuropathy | Diamond-Blackfan Anemia | Diarrhea | Diastrophic Dysplasia | DICER1 Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Diffuse Intrinsic Pontine Glioma | Diffuse Mesangial Sclerosis | Diffuse Palmoplantar Keratoderma | DiGeorge Syndrome | Discoid Lupus Erythematosus | Disseminated Intravascular Coagulation | Disseminated Superficial Actinic Porokeratosis | Distal Myopathy | Distal Myopathy 2 | Distal Spinal Muscular Atrophy | Diverticulitis | DNA Ligase IV Deficiency | DOCK8 Immunodeficiency Syndrome | Dominant Optic Atrophy | Donnai-Barrow Syndrome | Double Outlet Right Ventricle | Dowling-Degos Disease | Down Syndrome | DRESS Syndrome | Duane Retraction Syndrome | Dubin-Johnson Syndrome | Duchenne Muscular Dystrophy | Duodenal Atresia | Dupuytren Disease | Dwarfism | Dyggve-Melchior-Clausen Disease | Dysequilibrium Syndrome | Dysferlinopathy | Dysfibrinogenemia | Dyskeratosis Congenita | Dyslexia | Dyslipidemia | Dysmorphophobia | Dysplastic Nevus | Dysthymia | Dystonia | Dystonia Musculorum Deformans | Dystonia-parkinsonism, X-linked | Dystrophy, Cone-rod | Early Infantile Epileptic Encephalopathy | Early Infantile Epileptic Encephalopathy 1 | Early Infantile Epileptic Encephalopathy 13 | Early Infantile Epileptic Encephalopathy 28 | Early Infantile Epileptic Encephalopathy 4 | Eating Disorder | Ebstein Anomaly | Eccrine Porocarcinoma | Echinococcosis | Eclampsia | Ectodermal Dysplasia | Ectopia Lentis, Isolated, Autosomal Recessive | Ectrodactyly | Eczema | Ehlers-Danlos Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Eiken Syndrome | Ellis-Van Creveld Syndrome | Emery-Dreifuss Muscular Dystrophy | Empyema | Encephalitis | Encephalitis, Tick-borne | Encephalocele | Encephalopathy | Encephalopathy, Ethylmalonic | Encephalopathy, Glycine | Encephalopathy, Hepatic | Endocarditis | Endometrial Hyperplasia | Endometriosis | Endometritis | Endophthalmitis | Enhanced S-cone Syndrome | Enlarged Vestibular Aqueduct | Enterocolitis, Necrotizing | Eosinophilia | Eosinophilic Asthma | Ependymoma | Epicondylitis | Epidermal Nevus Syndrome | Epidermodysplasia Verruciformis | Epidermolysis Bullosa | Epidermolysis Bullosa Acquisita | Epidermolysis Bullosa Dystrophica | Epidermolysis Bullosa Simplex | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Epidermolysis Bullosa Simplex, Generalized | Epidermolysis Bullosa Simplex, Localized | Epidermolytic Hyperkeratosis | Epidermolytic Ichthyosis, Annular | Epidermolytic Palmoplantar Keratoderma | Epilepsy | Epilepsy Of Infancy With Migrating Focal Seizures | Epilepsy, Generalized | Epiphyseal Chondrodysplasia, Miura Type | Episodic Ataxia | Episodic Ataxia Type 1 | Episodic Ataxia Type 2 | Epithelial-myoepithelial Carcinoma | Epithelioid Hemangioma | Erdheim-Chester Disease | Erectile Dysfunction | Erysipelas | Erythema Multiforme | Erythema Nodosum | Erythematotelangiectatic Rosacea | Erythrokeratodermia Variabilis | Erythromelalgia | Erythropoietic Protoporphyria | Esophageal Adenocarcinoma | Esophageal Motility Disorders | Esophagitis | Essential Fructosuria | Esthesioneuroblastoma | Evans Syndrome | Exfoliative Dermatitis | Exocrine Pancreatic Insufficiency | Exostoses | Exotropia | Extramammary Paget's Disease | Fabry's Disease | Facioscapulohumeral Muscular Dystrophy | Facioscapulohumeral Muscular Dystrophy Type 1 | Facioscapulohumeral Muscular Dystrophy Type 2 | Fahr Disease | Familial Advanced Sleep Phase Syndrome | Familial Cerebral Amyloid Angiopathy | Familial Digital Arthropathy-brachydactyly | Familial Dysautonomia | Familial Episodic Pain Syndrome | Familial Exudative Vitreoretinopathy | Familial Glucocorticoid Deficiency | Familial Hemiplegic Migraine | Familial Hyperaldosteronism | Familial Hypertrophic Cardiomyopathy | Familial Hypobetalipoproteinemia | Familial Isolated Hyperparathyroidism | Familial Mediterranean Fever | Familial Partial Lipodystrophy | Familial Pheochromocytoma-paraganglioma | Familial Retinal Arterial Macroaneurysm | Familial Thoracic Aortic Aneurysm | Fanconi Anemia | Fanconi Syndrome | Farber Disease | Fascioliasis | Fatty Aldehyde Dehydrogenase Deficiency | Feingold Syndrome | Fetal Akinesia Deformation Sequence | Fetal Alcohol Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | FG Syndrome | Fibrillation, Atrial | Fibrodysplasia Ossificans Progressiva | Fibromuscular Dysplasia | Fibromyalgia | Fibronectin Glomerulopathy | Fibrosarcoma | Fibrosis | Filariasis | Focal Cortical Dysplasia Type 2 | Focal Dermal Hypoplasia | Focal Facial Dermal Dysplasia | Focal Segmental Glomerulosclerosis | Follicular Dendritic Cell Sarcoma | Fontaine Progeroid Syndrome | Fowler's Syndrome | Frank-ter Haar Syndrome | Frontometaphyseal Dysplasia | Frontotemporal Dementia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Fuchs Dystrophy | Fuchs Heterochromic Iridocyclitis | Fucosidosis | Fukuyama Congenital Muscular Dystrophy | Fundus Albipunctatus | Galactosemia | Galactosialidosis | Galloway-Mowat Syndrome | Gallstones | Ganglioglioma | Ganglioneuroma | Gangliosidosis | Gangliosidosis, GM1 | GAPO Syndrome | Gardner Syndrome | Gastric Atrophy | Gastritis | Gastritis, Atrophic | Gastroenteritis | Gastroenteritis, Eosinophilic | Gastrointestinal Disorders | Gastroschisis | GATA2 Deficiency | Gaucher Disease | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Genee-Wiedemann Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Generalized Epilepsy With Febrile Seizures Plus | Genitopatellar Syndrome | Gerodermia Osteodysplastica | Gerstmann-Straussler-Scheinker Syndrome | Gestational Trophoblastic Disease | Ghosal Syndrome | Giant Axonal Neuropathy | Giant Cell Arteritis | Giant Cell Glioblastoma | Gigantism | Gilbert Syndrome | Gingivitis | Gitelman Syndrome | Glanzmann Thrombasthenia | Glaucoma | Glaucoma, Congenital | Glaucomatocyclitic Crisis | Glioblastoma | Glioblastoma Multiforme | Glioma | Gliosarcoma | Globozoospermia | Glomerulonephritis | Glomerulonephritis, Membranoproliferative | Glomerulonephritis, Membranous | Glucagonoma | GLUT1 Deficiency Syndrome | Glutaric Aciduria Type 1 | Glutaric Aciduria Type 2 | Glutaric Aciduria Type 3 | Glutathione Synthetase Deficiency | Glycogen Storage Disease | Glycogen Storage Disease Type 0 | Glycogen Storage Disease Type 0, Muscle | Glycogen Storage Disease Type 1 | Glycogen Storage Disease Type 1a | Glycogen Storage Disease Type 1b | Glycogen Storage Disease Type 3 | Glycogen Storage Disease Type 4 | Glycogen Storage Disease Type 5 | Glycogen Storage Disease Type 6 | Glycogen Storage Disease Type 9 | GM2-gangliosidosis AB Variant | Gnathodiaphyseal Dysplasia | GNE Myopathy | Goiter | Goldenhar Syndrome | Gout | Graft-versus-host Disease | Granular Corneal Dystrophy | Granular Corneal Dystrophy Type 1 | Granuloma Annulare | Graves Disease | Gray Platelet Syndrome | Greenberg Dysplasia | Greig Cephalopolysyndactyly Syndrome | Growth Hormone Excess | Guanidinoacetate Methyltransferase Deficiency | Guillain-Barre Syndrome | Guttate Psoriasis | Gynecomastia | Gyrate Atrophy Of The Choroid And Retina | H Syndrome | Haim-Munk Syndrome | Hairy Cell Leukemia | Hamartoma | HANAC Syndrome | Hartnup Disease | Hartsfield Syndrome | Hashimoto Thyroiditis | Headache | Heart Block | Heart Failure | Heart Septal Defects