ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Familial Mediterranean Fever

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Familial Mediterranean Fever 55 coordinate concepts ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome \| ∟ Addison Disease \| ∟ Anemia, Hemolytic, Autoimmune \| ∟ Anti-Glomerular Basement Membrane Disease \| ∟ Antiphospholipid Syndrome \| ∟ Arthritis, Rheumatoid \| ∟ Autoimmune Diseases of the Nervous System \| ∟ Dermatitis Herpetiformis \| ∟ Diabetes Mellitus, Type 1 \| ∟ Glomerulonephritis, IGA \| ∟ Glomerulonephritis, Membranous \| ∟ Graves Disease \| ∟ Hepatitis, Autoimmune \| ∟ Lambert-Eaton Myasthenic Syndrome \| ∟ Lupus Erythematosus, Systemic \| ∟ Ophthalmia, Sympathetic \| ∟ Pemphigoid, Bullous \| ∟ Pemphigus \| ∟ Polyendocrinopathies, Autoimmune \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Reiter Syndrome \| ∟ Thyroiditis, Autoimmune Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Autoimmune Diseases ∟ Familial Mediterranean Fever 55 coordinate concepts ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome \| ∟ Addison Disease \| ∟ Anemia, Hemolytic, Autoimmune \| ∟ Anti-Glomerular Basement Membrane Disease \| ∟ Antiphospholipid Syndrome \| ∟ Arthritis, Rheumatoid \| ∟ Autoimmune Diseases of the Nervous System \| ∟ Dermatitis Herpetiformis \| ∟ Diabetes Mellitus, Type 1 \| ∟ Glomerulonephritis, IGA \| ∟ Glomerulonephritis, Membranous \| ∟ Graves Disease \| ∟ Hepatitis, Autoimmune \| ∟ Lambert-Eaton Myasthenic Syndrome \| ∟ Lupus Erythematosus, Systemic \| ∟ Ophthalmia, Sympathetic \| ∟ Pemphigoid, Bullous \| ∟ Pemphigus \| ∟ Polyendocrinopathies, Autoimmune \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Reiter Syndrome \| ∟ Thyroiditis, Autoimmune X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Familial Mediterranean Fever Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Autoimmune Diseases ∟ Familial Mediterranean Fever Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Autoimmune Diseases > Immune System Diseases > Medical Subject Headings (MeSH) X
Annotation:	a specific disease entity: do not use X ref PERIODIC DISEASE for periodically occurring dis ( = PERIODICITY (IM) + disease (IM)) X
historyNote*:	2000 (1966) X
publicMeSHNote*:	2000; see PERIODIC DISEASE 1966-1999; for FAMILIAL MEDITERRANEAN FEVER see PERIODIC DISEASE 1966-1999 X
Scope note:	An autosomal recessive inherited disease characterized by episodic FEVER; severe ABDOMINAL PAIN; PLEURISY; ARTHRITIS; and a characteristic ankle RASH. Disease flare-ups tend to last 3 days, and individuals are asymptomatic between attacks. ORCHITIS; benign recurrent MENINGITIS; HEADACHE; and AMYLOID nephropathy may also occur. (From Medicine (Baltimore) 1998 Jul;77(4):268-97) X
activeMeSHYear*:	2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	2004-07-07X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Adrenal Hyperplasia, Congenital \| Anemia, Hemolytic, Congenital \| Anemia, Hypoplastic, Congenital \| Ataxia Telangiectasia \| Blood Coagulation Disorders, Inherited \| Brugada Syndrome \| CADASIL \| Camurati-Engelmann Syndrome \| Cardiomyopathy, Hypertrophic, Familial \| Cherubism \| Chromosome Disorders \| Cystic Fibrosis \| Dwarfism \| Eye Diseases, Hereditary \| Genetic Diseases, X-Linked \| Genetic Diseases, Y-Linked \| Hajdu-Cheney Syndrome \| Hemoglobinopathies \| Heredodegenerative Disorders, Nervous System \| Hyperthyroxinemia, Familial Dysalbuminemic \| Jervell-Lange Nielsen Syndrome \| Kallmann Syndrome \| Kartagener Syndrome \| Marfan Syndrome \| Metabolism, Inborn Errors \| Muscular Dystrophies \| Myasthenic Syndromes, Congenital \| Nail-Patella Syndrome \| Neoplastic Syndromes, Hereditary \| Osteogenesis Imperfecta \| Pain Insensitivity, Congenital \| Romano-Ward Syndrome \| Skin Diseases, Genetic \| Werner Syndrome \| Addison Disease \| Anemia, Hemolytic, Autoimmune \| Anti-Glomerular Basement Membrane Disease \| Antiphospholipid Syndrome \| Arthritis, Rheumatoid \| Autoimmune Diseases of the Nervous System \| Dermatitis Herpetiformis \| Diabetes Mellitus, Type 1 \| Glomerulonephritis, IGA \| Glomerulonephritis, Membranous \| Graves Disease \| Hepatitis, Autoimmune \| Lambert-Eaton Myasthenic Syndrome \| Lupus Erythematosus, Systemic \| Ophthalmia, Sympathetic \| Pemphigoid, Bullous \| Pemphigus \| Polyendocrinopathies, Autoimmune \| Purpura, Thrombocytopenic, Idiopathic \| Reiter Syndrome \| Thyroiditis, Autoimmune X
URI:	X
Labels and equivalent concepts:	Perinnöllinen Välimeren kuume (fi) Suvuittainen välimerenkuume (fi, replaced) Suvuittainen Välimeren kuume (fi, replaced) Välimeren kuume (fi, replaced) Välimerenkuume (fi, replaced) Perinnöllinen välimerenkuume (fi, replaced) Familiaalinen välimerenkuume (fi, replaced) Familjär medelhavsfeber (sv) Periodic Disease, Wolff's (en, replaced) Periodic Disease (en, replaced) Periodic Fever Syndromes, Hereditary (en, replaced) Wolff Periodic Disease (en, replaced) Wolff's Periodic Disease (en, replaced) Mediterranean Fever, Familial (en, replaced) Febris Mediterranea familialis (la-FI, replaced) X
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