| 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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| hereditary hypertrophic n. |
progressive hypertrophic n.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary hypophosphatemic r. with hypercalciuria |
a form of familial hypophosphatemic rickets inherited as an autosomal trait; hypophosphatemia is accompanied by elevated levels of serum 1,25-dihydroxyvitamin D, increased intestinal absorption of calcium and phosphate, and hypercalciuria, indicating a defect in renal tubular function distinct from that of X-linked hypophosphatemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary iron-loading a. |
hereditary sideroblastic a.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary m. |
an autosomal recessive disease seen in young Afghan hounds, characterized by cavitation and necrosis of the white matter of the spinal cord, with pelvic limb paralysis before the age of one year.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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