| hereditary hemorrhagic telangiectasia |
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_hl_dorlands.jspz...
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| hereditary spastic paraplegia |
Hereditary spastic paraplegia (HSP), also called familial spastic paraparesis (FSP), refers to a group of inherited disorders that are characterized by progressive weakness and stiffness of the legs. Though the primary feature of HSP is severe, progressive, lower extremity spasticity, in more complicated forms it can be accompanied by other neurological symptoms. ...
출처: en.wikipedia.org/wiki/Hereditary_spastic_paraplegi...
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| hereditary disease |
A genetic disorder, or genetic disease is a disease caused, at least in part, by the genes of the person with the disease. There are a number of possible causes for genetic defects: * They may be caused by random mutation. * There are genetic disorders caused by the accidental duplication of a chromosome, as in Down syndrome and Klinefelter's syndrome, or repeated duplication of part of a chromosome as in Fragile X syndrome. ...
출처: en.wikipedia.org/wiki/Hereditary_disease
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| hereditary |
Transmitted from parent to child by information contained in the genes.
출처: www.stjude.org/glossary
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| hereditary |
Refers to a disease or condition that is passed from parents to child.
출처: www.bdid.com/termsh.htm
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