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        <rdfs:label>Familial Mediterranean Fever [Disease/Finding]</rdfs:label>
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        <ns2:Synonym>Periodic Disease, Wolff&#39;s</ns2:Synonym>
        <ns2:UMLS_CUI>C0031069</ns2:UMLS_CUI>
        <ns2:Synonym>Recurrent Polyserositis</ns2:Synonym>
        <ns2:Synonym>Benign Paroxysmal Peritonitis</ns2:Synonym>
        <ns2:Display_Name>Familial Mediterranean Fever</ns2:Display_Name>
        <ns2:Synonym>Periodic Peritonitis</ns2:Synonym>
        <ns2:MeSH_Definition>A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease.</ns2:MeSH_Definition>
        <ns2:Synonym>Mediterranean Fever, Familial</ns2:Synonym>
        <ns2:MeSH_Name>Familial Mediterranean Fever</ns2:MeSH_Name>
        <ns2:Synonym>Periodic Disease</ns2:Synonym>
        <ns2:RxNorm_CUI>1023411</ns2:RxNorm_CUI>
        <ns2:SNOMED_CID>12579009</ns2:SNOMED_CID>
        <ns2:Synonym>Wolff&#39;s Periodic Disease</ns2:Synonym>
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        <ns2:Synonym>Familial Paroxysmal Polyserositis</ns2:Synonym>
        <ns2:code>C4912</ns2:code>
        <ns2:MeSH_DUI>D010505</ns2:MeSH_DUI>
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        <ns2:MeSH_CUI>M0016320</ns2:MeSH_CUI>
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