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What is familial Mediterranean fever (FMF)?
What is the ICD 10 code for Mediterranean fever?
Is familial Mediterranean fever a disease?
What are the signs and symptoms of familial Mediterranean fever?
Nov 11, 2021 · Familial Mediterranean fever (FMF) is an inherited disorder that usually occurs in people of Mediterranean origin — including those of Jewish, Arab, Armenian, Turkish, North African, Greek or Italian ancestry. But it can affect people in any ethnic group. FMF is typically diagnosed during childhood.
Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder.: 149 FMF is an autoinflammatory disease caused by mutations in Mediterranean fever gene, which encodes a 781–amino acid protein called pyrin.
Oct 1, 2016 · ICD 10 code for Periodic fever syndromes. Get free rules, notes, crosswalks, synonyms, history for ICD-10 code M04.1.
Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles. ORPHA:342
Aug 31, 2022 · Last updated: 31 Aug 2022. Summary. Familial Mediterranean fever is primarily a genetic disease due to Mendelian-recessive inheritance of Mediterranean fever gene mutations. Occurs mainly in people of Mediterranean ancestry, especially from Arab countries, Turkey, Israel, and Armenia.
Familial Mediterranean fever is an inherited autoinflammatory syndrome characterised by recurrent short episodes of high fever associated with abdominal pain, inflammation of joints and other body sites and skin rash. If untreated, amyloidosis commonly develops and may have a fatal outcome.
Apr 12, 2022 · Familial Mediterranean fever (FMF) is characterized be episodes of fever, peritonitis and/or pleuritis. is an autosomal-recessive, hereditary auto-inflammatory disease and has a reference in the Online Mendelian Inheritance in Man database (OMIM) ID: 249100.
