| hereditary essential t. |
essential t.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary f. of bone |
osteogenesis imperfecta.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary fructose i. |
an autosomal recessive carbohydrate intolerance due to deficiency of fructose bisphosphate aldolase, isozyme B, with onset in infancy; it is characterized by hypoglycemia, with variable manifestations of fructosuria, fructosemia, anorexia, vomiting, failure to thrive, jaundice, splenomegaly, and an aversion to fructose-containing foods. If untreated, it may be fatal. See also essential fructosuria, under fructosuria.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary h. of neutrophils |
a hereditary condition in which the neutrophils are multilobed; called also Undritz anomaly.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary hemorrhagic t. |
an autosomal dominant vascular anomaly characterized by the presence of multiple small telangiectases of the skin, mucous membranes, gastrointestinal tract, and other organs, associated with recurrent episodes of bleeding from affected sites and gross or occult melena. Called also Osler's disease, Osler-Weber-Rendu disease, and Rendu-Osler-Weber syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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