Familial Mediterranean Fever
Familial Mediterranean Fever
About the Disease
Familial Mediterranean Fever, also known as periodic fever syndrome, is related to autoinflammation, panniculitis, and dermatosis syndrome and brucellosis, and has symptoms including abdominal pain, arthralgia and fever. An important gene associated with Familial Mediterranean Fever is MEFV (MEFV Innate Immunity Regulator, Pyrin), and among its related pathways/superpathways are Innate Immune System and Disease. The drugs Interleukin 1 Receptor Antagonist Protein and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, b cells and kidney, and related phenotypes are nausea and vomiting and constipation
Common Targets
Interleukin-1 (nonspecified subtype) | IL1B | FAM161A | IL-1 Receptor (nonspecified subtype) | MVK | G114548 | ABCG5 | NLRP3 Inflammasome | ZNF200 | PTPN22 | CXCR2 | MEFV | IL6R | HLA-DRB1 | TNFRSF1A | IL1RN | SAA1 | HLA-B | G5243 | Tubulin | CYP2D6 | MMP3

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Subacute Sclerosing Panencephalitis | Hyperinsulinemic Hypoglycemia | Multiple Myeloma | Hemangioendothelioma | Heart Failure | Macular Corneal Dystrophy | Thrombophilia | Hypertelorism | Anuria | Pompe Disease | Multiple Sclerosis, Relapsing-remitting | Limb Girdle Muscular Dystrophy | Combined Malonic And Methylmalonic Acidemia | Lentigo | Peeling Skin Syndrome, Acral Type | Pericarditis | Swine Influenza | Hypopigmentation | Cervicitis | Pontocerebellar Hypoplasia Type 7 | Congestive Heart Failure | Cavitary Optic Disc Anomalies | Familial Glucocorticoid Deficiency | Cerebrovascular Disorders | Familial Hemiplegic Migraine | Pycnodysostosis | Spinocerebellar Ataxia Type 38 | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Aneurysm, Thoracic Aortic | Fanconi Syndrome | Distal Myopathy | Proteus Syndrome | Milk Allergy | Chronic Beryllium Disease | Addison Disease | D-2-Hydroxyglutaric Aciduria | Carcinoid Syndrome | Sarcoma, Ewing | Generalized Epilepsy 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| Myocardial Infarction | Huntington's Disease | Progressive External Ophthalmoplegia | Cardiac Sarcoidosis | Erythrokeratodermia Variabilis | Personality Disorders | Burn-McKeown Syndrome | Sulfite Oxidase Deficiency | Hypokalemia | Learning Disability | Encephalitis, Tick-borne | Achromatopsia | Exocrine Pancreatic Insufficiency | Binge Eating Disorder | Dyslexia | Vestibular Disease | Fibronectin Glomerulopathy | Sarcoma, Alveolar Soft Part | Incontinentia Pigmenti | Plasma Cell Leukemia | Corneal Dystrophy | Transthyretin-related Amyloidosis | Coloboma | Canavan Disease | Actinomycetoma | Yellow Fever | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Thrombosis | Distal Spinal Muscular Atrophy | Toxic Epidermal Necrolysis | Antisocial Personality Disorder | Panniculitis | Progressive Encephalopathy-optic Atrophy Syndrome | Woodhouse-Sakati Syndrome | Myoclonus | Multiple Sclerosis, Primary Progressive | Speech Disorders | Periodontitis | Angioimmunoblastic T-cell Lymphoma | Birk-Barel Syndrome | Rhinitis | Ebstein Anomaly | Duchenne Muscular Dystrophy | Vulvovaginitis | Chronic Kidney Disease | Thin Basement Membrane Disease | Saethre-Chotzen Syndrome | Low Tension Glaucoma | Fundus Albipunctatus | Pemphigus | Paraganglioma | Supravalvular Aortic Stenosis | Polycystic Ovary Syndrome | Dyggve-Melchior-Clausen Disease | Cleidocranial Dysplasia | Birt-Hogg-Dube Syndrome | Jaundice, Obstructive | Liddle Syndrome | Blepharoconjunctivitis | Isovaleric Acidemia | Dementia | Mandibuloacral Dysplasia With Type A Lipodystrophy | Cutaneous Angiosarcoma | Gerodermia Osteodysplastica | Pneumococcal Meningitis | 3C Syndrome | Thrombasthenia | Arterial Tortuosity Syndrome | Behavioral Variant Of Frontotemporal Dementia | Thyroid Dyshormonogenesis | Otitis Media | Primary Hyperoxaluria Type 1 | Autosomal Recessive Spastic Paraplegia Type 75 | Split Hand-foot Malformation | Sialidosis Type I | Hypertensive Retinopathy | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Blastoma, Pleuropulmonary | Spinocerebellar Ataxia Type 16 | Tyrosinemia | Chitayat Syndrome | Cardiospondylocarpofacial Syndrome | Pregnancy, Ectopic | Neuroleptic Malignant Syndrome | Danon Disease | Dent Disease | Lymphoma, Mantle Cell | Nail-Patella Syndrome | Lewy Body Dementia | Sitosterolemia | Dysgerminoma | Acute Motor Axonal Neuropathy | Dementia, Vascular | Portal Vein Thrombosis | Fetal Alcohol Syndrome | Keloid | Hemochromatosis Type 2 | Gallstones | Polyarteritis Nodosa | Cystitis | Vitamin B12 Deficiency | Cold-induced Sweating Syndrome | Keratosis, Actinic | Mitochondrial Cytopathy | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Juvenile Xanthogranuloma | Acute Chest Syndrome | Platelet Disorders | Hepatitis, Autoimmune | Gastroschisis | Bacterial Meningitis | Sleep Apnea | Pulmonary Alveolar Microlithiasis | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | AIDS | Chiari Malformation Type I | Renal Hypouricemia | Inflammatory Joint Disease | Alopecia Totalis | T-cell Chronic Lymphocytic Leukemia | Cutaneous Lupus Erythematosus | Gray Platelet Syndrome | Von Willebrand Disease | Carpenter Syndrome | Disseminated Intravascular Coagulation | Nance-Horan Syndrome | Galactosialidosis | Hereditary Elliptocytosis | Hyperbilirubinemia, Neonatal | Sensory Neuropathy | Sponastrime Dysplasia | Cancer, Brain | Pseudohypoparathyroidism Type 1A | Stroke, Hemorrhagic | Anti-NMDA Receptor Encephalitis | Hereditary Sensory And Autonomic Neuropathy | Weill-Marchesani Syndrome | Neuromuscular Disorders | Esophageal Adenocarcinoma | Progressive Familial Intrahepatic Cholestasis Type 2 | Cerebral Cavernous Malformations | Postpartum Depression | Greenberg Dysplasia | Granular Corneal Dystrophy Type 1 | Bicuspid Aortic Valve | Glycogen Storage Disease Type 5 | Loeys-Dietz Syndrome Type 4 | Restless Legs Syndrome | Bronchitis, Chronic | Glycogen Storage Disease Type 4 | Heavy Chain Disease | Paraganglioma, Carotid Body | Osteogenesis Imperfecta Type VI | Bartsocas-Papas Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Vici Syndrome | Cramp Fasciculation Syndrome | Hypertension | Retinal Degeneration | Miyoshi Myopathy | Acrodermatitis Enteropathica | Familial Partial Lipodystrophy | Myelitis, Transverse | Macrophage Activation Syndrome | Osteonecrosis Of The Jaw | Congenital Lipoid Adrenal Hyperplasia | Blue Nevus | Microcephalic Primordial Dwarfism | Polycythemia Vera | Adenomatoid Tumor | Syphilis | Fowler's Syndrome | Overactive Bladder | Sengers Syndrome | Adenocarcinoma | Hepatitis D | Lymphomatoid Granulomatosis | Torticollis | Hypertension, Pulmonary | Diffuse Intrinsic Pontine Glioma | Nephritis, Interstitial | Infertility | Charcot-Marie-Tooth Disease, Type 6 | Protein C Deficiency | Pituitary Dwarfism | Eiken Syndrome | Fraser Syndrome | Colorectal Adenoma | Influenza | Spinocerebellar Ataxia Type 20 | Charcot-Marie-Tooth Disease Type 2T | Microcephaly, Seizures, And Developmental Delay | LMNA-related 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