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1. • L70.0

     • L70.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
     www.icd10data.com/ICD10CM/Codes/L00-L99/L60-L75/L70-/L70.0

     2025 ICD-10-CM Diagnosis Code L70.0: Acne vulgaris

2. People also ask

   What is familial Mediterranean fever?

   • 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.

   Familial Mediterranean fever - DermNet

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   Is Mediterranean fever autosomal dominant?

   • There is a less common autosomal dominant form (MIM 134610). Familial Mediterranean fever is usually due to mutations in the Mediterranean fever (MEFV) or pyrin gene located on chromosome 16 (16p13.3). Mutations in the MEFV gene have been found in 80% of typical cases. More than 100 different disease-linked mutations have been identified.

   Familial Mediterranean fever - DermNet

   dermnetnz.org/topics/familial-mediterranean-fever

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   What happens if familial Mediterranean fever is not treated?

   • Untreated familial Mediterranean fever can result in serious complications such as end-stage renal disease and malabsorption secondary to amyloid deposition in the kidneys and digestive tract, male and female infertility, and growth retardation in children.

   Diagnosis and management of familial Mediterranean fever: Integrating

   www.gimjournal.org/article/S1098-3600(21)00144-1/fulltext

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   What causes Mediterranean fever?

   • Virtually all cases are due to a mutation in the Mediterranean Fever (MEFV) gene on the chromosome 16, which codes for a protein called pyrin or marenostrin. Various mutations of this gene lead to FMF, although some mutations cause a more severe picture than others. Mutations occur mainly in exons 2, 3, 5 and 10.

   Familial Mediterranean fever - Wikipedia

   en.wikipedia.org/wiki/Familial_Mediterranean_fever

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   When does a child develop Mediterranean fever?

   • Two-thirds of patients develop symptoms before the age of 5 years and 90% by 20 years of age. Familial Mediterranean fever is usually inherited as an autosomal recessive condition, meaning both parents must carry the defective gene and there is a one in four chance of a child being affected (MIM 249100).

   Familial Mediterranean fever - DermNet

   dermnetnz.org/topics/familial-mediterranean-fever

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   How is familial Mediterranean fever diagnosed?

   • Diagnosis of familial Mediterranean fever is made using the Tel-Hashomer criteria: The diagnosis if definite if 2 major or 1 major + 2 minor criteria are met. The diagnosis is probable if 1 major + 1 minor criteria are met. Blood tests during an attack may show: Increased serum IgD in 10%.

   Familial Mediterranean fever - DermNet

   dermnetnz.org/topics/familial-mediterranean-fever

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3. dermnetnz.org › topics › familial-mediterranean-feverFamilial Mediterranean fever - DermNet

   dermnetnz.org › topics › familial-mediterranean-fever

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   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.

4. bestpractice.bmj.com › topics › en-gbFamilial Mediterranean fever - Symptoms, diagnosis and ...

   bestpractice.bmj.com › topics › en-gb

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   Sep 30, 2010 · 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.

5. www.gimjournal.org › article › S1098-3600(21)00144-1Diagnosis and management of familial Mediterranean fever ...

   www.gimjournal.org › article › S1098-3600(21)00144-1

   Familial Mediterranean fever (FMF) is an autosomal recessive systemic autoinflammatory disorder characterized by recurrent episodes of fever accompanied by peritonitis, pleuritis, pericarditis, and/or arthritis, sometimes accompanied by an erysipelas-like skin rash.

6. gpnotebook.com › familial-mediterranean-feverFamilial mediterranean fever – GPnotebook

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   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. FMF occurs as a result of mutations in the MEditerranean FeVer (MEFV gene)

7. www.rheumaknowledgy.com › familial-mediterraneanRheumaKnowledgy » Familial Mediterranean Fever (FMF)

   www.rheumaknowledgy.com › familial-mediterranean

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   Nov 5, 2014 · icd-10: e85.0 Definition: FMF is an intermittent febrile disorder with inflammatory serositis, arthritis, and rash. Etiology: FMF is an autosomal recessive disorder associated.

8. dermnetnz.org › topics › periodic-fever-syndromesPeriodic fever syndromes - DermNet

   dermnetnz.org › topics › periodic-fever-syndromes

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   Familial Mediterranean fever (FMF): MIM 249100. Hyperimmunoglobulinaemia D syndrome (hyperIgD syndrome, HIDS): MIM 260920. Autosomal dominant periodic fever syndromes. Only a single copy of the defective gene is required to develop symptoms and signs of an autosomal dominant periodic fever syndrome.

9. en.wikipedia.org › wiki › Familial_Mediterranean_feverFamilial Mediterranean fever - Wikipedia

   en.wikipedia.org › wiki › Familial_Mediterranean_fever

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   Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder. [1]: 149 FMF is an autoinflammatory disease caused by mutations in Mediterranean fever gene, which encodes a 781–amino acid protein called pyrin. [2] .