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to be hereditary

См. также в других словарях:

  • Hereditary elliptocytosis — Classification and external resources Blood smear showing elliptocytes ICD 10 D …   Wikipedia

  • Hereditary hemorrhagic telangiectasia — Classification and external resources Characteristic lip telangiectases. ICD 10 I …   Wikipedia

  • Hereditary multiple exostoses — Classification and external resources Photograph of the legs of a 26 year old male showing multiple lumps leading to deformity. ICD 10 Q …   Wikipedia

  • Hereditary peer — Hereditary peers form part of the Peerage in the United Kingdom. There are over seven hundred peers who hold titles that may be inherited. Formerly, most of them were entitled to a seat in House of Lords, but since the House of Lords Act 1999… …   Wikipedia

  • Hereditary nonpolyposis colorectal cancer — Classification and external resources ICD 10 C18 C20 ICD 9 …   Wikipedia

  • Hereditary coproporphyria — Classification and external resources Coproporphyrinogen III ICD 10 E …   Wikipedia

  • Hereditary title — Hereditary titles, in a general sense, are titles, positions or styles that are hereditary and thus tend or are bound to remain in particular families. Some hereditary titles are inherited only by the eldest son (see primogeniture) [cite web|… …   Wikipedia

  • hereditary — he·red·i·tary /hə re də ˌter ē/ adj [Latin hereditarius, from hereditas inheritance, from hered heres heir] 1: received or passing by inheritance or required to pass by inheritance hereditary shares 2: having ownership or possession through… …   Law dictionary

  • Hereditary mucoepithelial dysplasia — Classification and external resources ICD 10 L98.9 ICD 9 709.9 …   Wikipedia

  • Hereditary inclusion body myopathy — Hereditary inclusion body myopathies (HIBM) are a heterogeneous group of genetic disorders which have different symptoms. Generally, they are neuromuscular disorders characterized by muscle weakness developing in young adults. Hereditary… …   Wikipedia

  • Hereditary equine regional dermal asthenia — (HERDA) aka hyperelastosis cutis (HC) is an inherited autosomal recessive connective tissue disorder. It develops from a homozygous recessive mutation that weakens collagen fibers that allow the skin of the animal to stay connected to the rest of …   Wikipedia

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