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- Wilson's_disease abstract "Wilson's disease or hepatolenticular degeneration is an autosomal recessive genetic disorder in which copper accumulates in tissues; this manifests as neurological or psychiatric symptoms and liver disease. It is treated with medication that reduces copper absorption or removes the excess copper from the body, but occasionally a liver transplant is required.The condition is due to mutations in the Wilson disease protein (ATP7B) gene. A single abnormal copy of the gene is present in 1 in 100 people, who do not develop any symptoms (they are carriers). If a child inherits the gene from both parents, the child may develop Wilson's disease. Symptoms usually appear between the ages of 6 and 20 years, but cases in much older people have been described. Wilson's disease occurs in 1 to 4 per 100,000 people. It is named after Samuel Alexander Kinnier Wilson (1878–1937), the British neurologist who first described the condition in 1912.".
- Wilson's_disease diseasesdb "14152".
- Wilson's_disease emedicineSubject "med".
- Wilson's_disease emedicineTopic "2413".
- Wilson's_disease icd10 "E83.0".
- Wilson's_disease icd9 "275.1".
- Wilson's_disease medlineplus "000785".
- Wilson's_disease meshId "D006527".
- Wilson's_disease omim "277900".
- Wilson's_disease thumbnail Kayser-Fleischer_ring.jpg?width=300.
- Wilson's_disease wikiPageExternalLink www.childliverdisease.org.
- Wilson's_disease wikiPageExternalLink index.php.
- Wilson's_disease wikiPageExternalLink www.wilsonsdisease.org.uk.
- Wilson's_disease wikiPageExternalLink www.wilsonsdisease.org.
- Wilson's_disease wikiPageID "60138".
- Wilson's_disease wikiPageRevisionID "605036579".
- Wilson's_disease caption "A Kayser-Fleischer ring is common in Wilson's disease, especially when neurological symptoms are present".
- Wilson's_disease diseasesdb "14152".
- Wilson's_disease emedicinesubj "med".
- Wilson's_disease emedicinetopic "2413".
- Wilson's_disease genereviewsname "Wilson Disease".
- Wilson's_disease genereviewsnbk "NBK1512".
- Wilson's_disease hasPhotoCollection Wilson's_disease.
- Wilson's_disease icd "275.1".
- Wilson's_disease icd "E83.0".
- Wilson's_disease medlineplus "785".
- Wilson's_disease meshid "D006527".
- Wilson's_disease name "Wilson's disease".
- Wilson's_disease omim "277900".
- Wilson's_disease wordnet_type synset-disease-noun-1.
- Wilson's_disease subject Category:Autosomal_recessive_disorders.
- Wilson's_disease subject Category:Diseases_of_liver.
- Wilson's_disease subject Category:Hepatology.
- Wilson's_disease subject Category:Neurological_disorders.
- Wilson's_disease subject Category:Rare_diseases.
- Wilson's_disease type Abstraction100002137.
- Wilson's_disease type Attribute100024264.
- Wilson's_disease type AutosomalRecessiveDisorders.
- Wilson's_disease type Condition113920835.
- Wilson's_disease type Disease114070360.
- Wilson's_disease type Disorder114052403.
- Wilson's_disease type IllHealth114052046.
- Wilson's_disease type Illness114061805.
- Wilson's_disease type NervousDisorder114084880.
- Wilson's_disease type NeurologicalDisorders.
- Wilson's_disease type PathologicalState114051917.
- Wilson's_disease type PhysicalCondition114034177.
- Wilson's_disease type State100024720.
- Wilson's_disease type Disease.
- Wilson's_disease type AilmentCondition.
- Wilson's_disease type Situation.
- Wilson's_disease comment "Wilson's disease or hepatolenticular degeneration is an autosomal recessive genetic disorder in which copper accumulates in tissues; this manifests as neurological or psychiatric symptoms and liver disease. It is treated with medication that reduces copper absorption or removes the excess copper from the body, but occasionally a liver transplant is required.The condition is due to mutations in the Wilson disease protein (ATP7B) gene.".
- Wilson's_disease label "Choroba Wilsona".
- Wilson's_disease label "Doença de Wilson".
- Wilson's_disease label "Enfermedad de Wilson".
- Wilson's_disease label "Maladie de Wilson".
- Wilson's_disease label "Malattia di Wilson".
- Wilson's_disease label "Morbus Wilson".
- Wilson's_disease label "Wilson's disease".
- Wilson's_disease label "Ziekte van Wilson".
- Wilson's_disease label "Болезнь Вильсона — Коновалова".
- Wilson's_disease label "داء ويلسون".
- Wilson's_disease label "肝レンズ核変性症".
- Wilson's_disease label "肝豆狀核變性".
- Wilson's_disease sameAs Wilsonova_choroba.
- Wilson's_disease sameAs Morbus_Wilson.
- Wilson's_disease sameAs Νόσος_του_Γουίλσον.
- Wilson's_disease sameAs Enfermedad_de_Wilson.
- Wilson's_disease sameAs Maladie_de_Wilson.
- Wilson's_disease sameAs Malattia_di_Wilson.
- Wilson's_disease sameAs 肝レンズ核変性症.
- Wilson's_disease sameAs 윌슨병.
- Wilson's_disease sameAs Ziekte_van_Wilson.
- Wilson's_disease sameAs Choroba_Wilsona.
- Wilson's_disease sameAs Doença_de_Wilson.
- Wilson's_disease sameAs m.0gcdl.
- Wilson's_disease sameAs Q117121.
- Wilson's_disease sameAs Q117121.
- Wilson's_disease sameAs 1198.
- Wilson's_disease sameAs Wilson's_disease.
- Wilson's_disease wasDerivedFrom Wilson's_disease?oldid=605036579.
- Wilson's_disease depiction Kayser-Fleischer_ring.jpg.
- Wilson's_disease isPrimaryTopicOf Wilson's_disease.
- Wilson's_disease name "Wilson's disease".
