| familial amyloid p. |
autosomal dominant amyloid polyneuropathy occurring in hereditary amyloidosis; major subtypes are Portuguese type familial amyloid p., Indiana type familial amyloid p., and Finnish type familial amyloid p.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial apolipoprotein C-II (apo C-II) d. |
an autosomal recessive disorder due to lack of apo C-II, a necessary cofactor for lipoprotein lipase. It results in familial hyperchylomicronemia that is usually milder and of later onset than that caused by a defect in the enzyme itself. See also table at hyperlipoproteinemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial autonomic d. |
familial dysautonomia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial benign chronic n. |
chronic benign n.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial c. |
familial chloride diarrhea.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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