| familial a. |
a concentration of cases of a disease in families; the occurrence of more cases of a given disorder in close relatives of a person with the disorder than in control families.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
|---|---|
| familial acholuric j. |
hereditary spherocytosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| familial alobar h. |
a form in which the chromosomes are normal but otherwise resembling that due to trisomy 13 (see holoprosencephaly).
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| 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...
|
| 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...
|