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hereditary hemorrhagic telangiectasia

См. также в других словарях:

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

  • Hereditary hemorrhagic telangiectasia — A genetic disease characterized by the presence of multiple direct connections between arteries and veins called arteriovenous malformations (AVMs). The small AVMs close to the surface of skin and mucous membranes (as in the mouth) are the… …   Medical dictionary

  • Telangiectasia, hereditary hemorrhagic — A genetic disease characterized by the presence of multiple direct connections between arteries and veins called arteriovenous malformations (AVMs). The small AVMs close to the surface of skin and mucous membranes (as in the mouth) are the… …   Medical dictionary

  • Telangiectasia — Classification and external resources ICD 10 G11.3, I …   Wikipedia

  • telangiectasia — Dilation of the previously existing small or terminal vessels of a part. SYN: angiotelectasis, angiotelectasia. [G. telos, end, + angeion, vessel, + ektasis, a stretching out] cephalo oculocutaneous t. an angioma involving the skin of the face,… …   Medical dictionary

  • Goldstein disease — hereditary hemorrhagic telangiectasia …   Medical dictionary

  • Osler-Weber-Rendu disease — hereditary hemorrhagic telangiectasia …   Medical dictionary

  • Rendu-Osler-Weber syndrome — hereditary hemorrhagic telangiectasia …   Medical dictionary

  • HHT — Hereditary Hemorrhagic Telangiectasia (Medical » Physiology) * Headquarters and Headquarters Troop (Governmental » US Government) * Headquarters and Headquarters Troop (Governmental » Military) …   Abbreviations dictionary

  • List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… …   Wikipedia

  • ACVRL1 — Activin A receptor type II like 1, also known as ACVRL1, is a human gene.cite web | title = Entrez Gene: ACVRL1 activin A receptor type II like 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=94|… …   Wikipedia

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