| familial lipoprotein d. |
any inherited disorder of lipoprotein metabolism resulting in deficiency of one or more plasma lipoproteins; see abetalipoproteinemia, Tangier disease under disease, and hypobetalipoproteinemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial m. |
Meyer-Betz disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial Mediterranean f. |
a hereditary, autosomal recessive disease usually occurring in Armenians and Sephardic Jews, caused by mutation of a gene on chromosome 16p that codes for the protein pyrin, and characterized by short recurrent attacks of fever with pain in the abdomen, chest, or joints and erythema resembling that seen in erysipelas; it is sometimes complicated by reactive systemic amyloidosis (q.v.). Called also benign paroxysmal peritonitis, periodic peritonitis, familial recurrent polyserositis, and periodic or recurrent polyserositis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial o. |
Morquio's syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial o. of fingers |
Thiemann's disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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