| familial hemiplegic m. |
a rare type of hemiplegic migraine that is passed on as an autosomal dominant trait.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| familial hemophagocytic r. |
histiocytic medullary r.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial Hibernian f. |
TNF-receptor–associated periodic syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial high-density lipoprotein (HDL) d. |
any of several inherited disorders of lipoprotein and lipid metabolism that result in decreased plasma levels of high-density lipoproteins, particularly Tangier disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial hypocalciuric h. |
an autosomal dominant type of hypercalcemia with vague and mild symptoms.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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