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- Von_Willebrand_disease abstract "Von Willebrand disease (vWD) (/ˌfʌnˈvɪlɨbrɑːnt/) is the most common hereditary coagulation abnormality described in humans, although it can also be acquired as a result of other medical conditions. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. It is known to affect humans and dogs (notably Doberman Pinschers), and rarely swine, cattle, horses, and cats. There are three forms of vWD: hereditary, acquired, and pseudo or platelet type. There are three types of hereditary vWD: vWD Type I, vWD Type II, and vWD Type III. Within the three inherited types of vWD there are various subtypes. Platelet type vWD is also an inherited condition.vWD Type I is the most common type of the disorder and those that have it are typically asymptomatic or may experience mild symptoms such as nosebleeds although there may be severe symptoms in some cases. There are various factors that affect the presentation and severity of symptoms of vWD such as blood type.vWD is named after Erik Adolf von Willebrand, a Finnish pediatrician who first described the disease in 1926.".
- Von_Willebrand_disease icd10 "D68.0".
- Von_Willebrand_disease icd9 "286.4".
- Von_Willebrand_disease meshId "D014842".
- Von_Willebrand_disease omim "193400".
- Von_Willebrand_disease wikiPageExternalLink annurev.biochem.67.1.395.
- Von_Willebrand_disease wikiPageExternalLink pmidlookup?view=short&pmid=15306670&promo=ONFLNS19.
- Von_Willebrand_disease wikiPageExternalLink openurl?genre=article&sid=nlm:pubmed&issn=1351-8216&date=2004&volume=10&issue=3&spage=199.
- Von_Willebrand_disease wikiPageExternalLink www.haemophilia.org.uk.
- Von_Willebrand_disease wikiPageExternalLink www.hemophilia.org.
- Von_Willebrand_disease wikiPageExternalLink br.fcgi?book=gene&part=von-willebrand.
- Von_Willebrand_disease wikiPageExternalLink index.htm.
- Von_Willebrand_disease wikiPageExternalLink vwf.
- Von_Willebrand_disease wikiPageExternalLink www.ukhcdo.org.
- Von_Willebrand_disease wikiPageExternalLink www.wfh.org.
- Von_Willebrand_disease wikiPageID "311436".
- Von_Willebrand_disease wikiPageRevisionID "643238371".
- Von_Willebrand_disease diseasesdb "14007".
- Von_Willebrand_disease emedicinesubj "ped".
- Von_Willebrand_disease emedicinetopic "2419".
- Von_Willebrand_disease field Hematology.
- Von_Willebrand_disease genereviewsname "von Willebrand Disease".
- Von_Willebrand_disease genereviewsnbk "NBK7014".
- Von_Willebrand_disease hasPhotoCollection Von_Willebrand_disease.
- Von_Willebrand_disease icd "286.4".
- Von_Willebrand_disease icd "D68.0".
- Von_Willebrand_disease medlineplus "544".
- Von_Willebrand_disease meshid "D014842".
- Von_Willebrand_disease name "von Willebrand disease".
- Von_Willebrand_disease omim "193400".
- Von_Willebrand_disease wordnet_type synset-disease-noun-1.
- Von_Willebrand_disease subject Category:Autosomal_dominant_disorders.
- Von_Willebrand_disease subject Category:Coagulopathies.
- Von_Willebrand_disease type Abstraction100002137.
- Von_Willebrand_disease type Attribute100024264.
- Von_Willebrand_disease type AutosomalDominantDisease114162025.
- Von_Willebrand_disease type AutosomalDominantDisorders.
- Von_Willebrand_disease type Condition113920835.
- Von_Willebrand_disease type Disease114070360.
- Von_Willebrand_disease type GeneticDisease114151139.
- Von_Willebrand_disease type IllHealth114052046.
- Von_Willebrand_disease type Illness114061805.
- Von_Willebrand_disease type PathologicalState114051917.
- Von_Willebrand_disease type PhysicalCondition114034177.
- Von_Willebrand_disease type State100024720.
- Von_Willebrand_disease type Disease.
- Von_Willebrand_disease type Medicine.
- Von_Willebrand_disease type AilmentCondition.
- Von_Willebrand_disease type Thing.
- Von_Willebrand_disease type Q12136.
- Von_Willebrand_disease comment "Von Willebrand disease (vWD) (/ˌfʌnˈvɪlɨbrɑːnt/) is the most common hereditary coagulation abnormality described in humans, although it can also be acquired as a result of other medical conditions. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. It is known to affect humans and dogs (notably Doberman Pinschers), and rarely swine, cattle, horses, and cats.".
- Von_Willebrand_disease label "Choroba von Willebranda".
- Von_Willebrand_disease label "Doença de Von Willebrand".
- Von_Willebrand_disease label "Enfermedad de von Willebrand".
- Von_Willebrand_disease label "Maladie de Willebrand".
- Von_Willebrand_disease label "Malaltia de von Willebrand".
- Von_Willebrand_disease label "Malattia di von Willebrand".
- Von_Willebrand_disease label "Von Willebrand disease".
- Von_Willebrand_disease label "Von Willebrand–Jürgens-szindróma".
- Von_Willebrand_disease label "Von Willebrant hastalığı".
- Von_Willebrand_disease label "Willebrand-Jürgens-Syndrom".
- Von_Willebrand_disease label "Болезнь Виллебранда".
- Von_Willebrand_disease label "ヴォン・ヴィレブランド病".
- Von_Willebrand_disease sameAs Willebrand-Jürgens-Syndrom.
- Von_Willebrand_disease sameAs Enfermedad_de_von_Willebrand.
- Von_Willebrand_disease sameAs Maladie_de_Willebrand.
- Von_Willebrand_disease sameAs Malattia_di_von_Willebrand.
- Von_Willebrand_disease sameAs ヴォン・ヴィレブランド病.
- Von_Willebrand_disease sameAs Choroba_von_Willebranda.
- Von_Willebrand_disease sameAs Doença_de_Von_Willebrand.
- Von_Willebrand_disease sameAs m.01t787.
- Von_Willebrand_disease sameAs Q709360.
- Von_Willebrand_disease sameAs Q709360.
- Von_Willebrand_disease sameAs 1258.
- Von_Willebrand_disease sameAs 4147.
- Von_Willebrand_disease sameAs C0042974.
- Von_Willebrand_disease sameAs Von_Willebrand_disease.
- Von_Willebrand_disease wasDerivedFrom Von_Willebrand_disease?oldid=643238371.
- Von_Willebrand_disease isPrimaryTopicOf Von_Willebrand_disease.
- Von_Willebrand_disease name "von Willebrand disease".