C0013720 - An inherited connective tissue disorder characterized by loose and fragile skin and joint hypermobility. 2/10
home    UMLS 2020

293,031 терминов и синонимов из MeSH и LOINC

Поиск по CUI
Поиск по CODE


Поиск по одному или нескольким словам или частям слов
   


Lang   Dictionary       CODE         LUI      
preferred
no
       SUI   preference
Yes / No
Terms, descriptions
CUI    C0013720
RussianMedical Subject Headings Russian D004535 L3377498preferred S3904991 Y ЭЛЕРСА-ДАНЛОСА СИНДРОМ
RussianMedical Subject Headings Russian D004535 L0892836no S1096653 Y ELERSA-DANLOSA SINDROM
RussianMedical Subject Headings Russian D004535 L1515223no S1811132 Y DESMOGENEZ NESOVERSHENNYI
RussianMDRRUS 10011691 L15723218no S19027909 Y Гиперпластическая кожа
RussianMDRRUS 10014316 L15763049no S19079706 N Синдром Эхлерса-Данлоса
RussianMDRRUS 10014316 L15763049no S19079706 Y Синдром Эхлерса-Данлоса
RussianMedical Subject Headings Russian D004535 L3347317no S3874795 Y ДЕСМОГЕНЕЗ НЕСОВЕРШЕННЫЙ
Medical Subject Headings A0053087 AT115063143 A heterogeneous group of autosomally inherited COLLAGEN DISEASES caused by defects in the synthesis or structure of FIBRILLAR COLLAGEN. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability.
(CPTSP) CRISP Thesaurus A0409879 AT51221404 group of inherited disorders of the connective tissue; major manifestations include hyperextensible skin and joints, easy bruisability, friability of tissues with bleeding and poor wound healing, calcified subcutaneous spheroids, and pseudotumors.
Medical Subject Headings Czech A13069890 AT156611350 Dědičné onemocnění s porušenou tvorbou kolagenu, které se projevuje nápadnou volností kloubů, hyperelastičností a zranitelností kůže; často bývá postižena rovněž pojivová tkáň vnitřních orgánů. (cit. Velký lékařský slovník online, 2012 http://lekarske.slovniky.cz/ )
MEDLINEPLUS A21142626 AT220107311

Ehlers-Danlos syndrome (EDS) is a group of inherited disorders that weaken connective tissues. Connective tissues are proteins that support skin, bones, blood vessels, and other organs.

EDS usually affects your skin, joints and blood vessel walls. Symptoms include

  • Loose joints
  • Fragile, small blood vessels
  • Abnormal scar formation and wound healing
  • Soft, velvety, stretchy skin that bruises easily

There are several types of EDS. They can range from mild to life-threatening. About 1 in 5,000 people has EDS. There is no cure. Treatment involves managing symptoms, often with medicines and physical therapy. It also includes learning how to protect your joints and prevent injuries.

MSHNOR A21185482 AT221577030 En heterogen gruppe av autosomalt arvelige kollagene sykdommer forårsaket av defekter i syntesen eller strukturen av fibrillært kollagen. Det er tallrike subtyper: klassisk, hypermobil, vaskulær og andre. Vanlige kliniske trekk inkluderer hud og ledd som kan strekkes mer enn vanlig, skjørhet av huden og redusert sårtilheling.
NCI Thesaurus A7570226 AT198115869 An inherited connective tissue disorder characterized by loose and fragile skin and joint hypermobility.