%D9%85%D8%B1%D8%B6_%D8%A7%D9%84%D9%83%D9%84%D9%89_%D8%A7%D9%84%D9%85%D8%AA%D8%B9%D8%AF%D8%AF_%D8%A7%D9%84%D9%83%D9%8A%D8%B3%D8%A7%D8%AAPoliquistosi_renalCategory:Polycystic_kidney_diseaseZystennierePolycystic_kidney_disease%D8%A8%DB%8C%D9%85%D8%A7%D8%B1%DB%8C_%DA%A9%D9%84%DB%8C%D9%87_%D9%BE%D9%84%DB%8C%E2%80%8C%DA%A9%DB%8C%D8%B3%D8%AA%DB%8C%DA%A9%D7%9E%D7%97%D7%9C%D7%AA_%D7%9B%D7%9C%D7%99%D7%95%D7%AA_%D7%A4%D7%95%D7%9C%D7%99%D7%A6%D7%99%D7%A1%D7%98%D7%99%D7%AAMalattia_policistica_renale%E5%A4%9A%E7%99%BA%E6%80%A7%E5%9A%A2%E8%83%9E%E8%85%8E%D0%91%D2%AF%D0%B9%D1%80%D0%B5%D0%BA%D1%82%D0%B5%D0%B3%D1%96_%D0%BA%D0%B8%D1%81%D1%82%D0%B0_%D0%B0%D1%83%D1%80%D1%83%D0%BB%D0%B0%D1%80%D1%8B%EB%8B%A4%EB%82%AD%EC%84%B1_%EC%8B%A0%EC%A2%85Wielotorbielowato%C5%9B%C4%87_nerekDoen%C3%A7a_do_rim_polic%C3%ADstico%D0%9F%D0%BE%D0%BB%D0%B8%D0%BA%D0%B8%D1%81%D1%82%D0%BE%D0%B7_%D0%BF%D0%BE%D1%87%D0%B5%D0%BA%D0%9F%D0%BE%D0%BB%D0%B8%D1%86%D0%B8%D1%81%D1%82%D0%B8%D1%87%D0%BD%D0%B0_%D0%B1%D0%BE%D0%BB%D0%B5%D1%81%D1%82_%D0%B1%D1%83%D0%B1%D1%80%D0%B5%D0%B3%D0%B0Polycystisk_njursjukdom%D0%9F%D0%BE%D0%BB%D1%96%D0%BA%D1%96%D1%81%D1%82%D0%BE%D0%B7_%D0%BD%D0%B8%D1%80%D0%BE%D0%BAQ15443105%E5%A4%9A%E5%9B%8A%E8%85%8E%E5%A4%9A%E5%9B%8A%E6%80%A7%E8%85%8E%E7%97%85%E8%AE%8A
about
P509
Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2)Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1Interventions for preventing the progression of autosomal dominant polycystic kidney diseaseInterventions for infected cysts in people with autosomal dominant polycystic kidney diseaseInterventions for preventing the progression of autosomal dominant polycystic kidney diseasePolycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channelCpG island in the region of an autosomal dominant polycystic kidney disease locus defines the 5' end of a gene encoding a putative proton channelThe NTN2L gene encoding a novel human netrin maps to the autosomal dominant polycystic kidney disease region on chromosome 16p13.3A novel ribosomal protein L3-like gene (RPL3L) maps to the autosomal dominant polycystic kidney disease gene regionCleavage of polycystin-1 requires the receptor for egg jelly domain and is disrupted by human autosomal-dominant polycystic kidney disease 1-associated mutations.Autosomal dominant polycystic kidney disease: the last 3 yearsCardiovascular abnormalities in autosomal-dominant polycystic kidney diseaseA spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney Disorders and European Renal Best PracticeCurrent management of autosomal dominant polycystic kidney diseaseA systematic review of the predictors of disease progression in patients with autosomal dominant polycystic kidney diseaseVascular complications in autosomal dominant polycystic kidney diseaseThyroid-like follicular carcinoma of the kidney in a patient with nephrolithiasis and polycystic kidney disease: a case reportShould patients with autosomal dominant polycystic kidney disease be screened for cerebral aneurysms?Spanish guidelines for the management of autosomal dominant polycystic kidney diseaseClinical Trials in Autosomal Dominant Polycystic Kidney DiseaseTherapeutic Area Data Standards for Autosomal Dominant Polycystic Kidney Disease: A Report From the Polycystic Kidney Disease Outcomes Consortium (PKDOC)Novel role of ouabain as a cystogenic factor in autosomal dominant polycystic kidney diseaseExtra-renal manifestations of autosomal dominant polycystic kidney disease (ADPKD): considerations for routine screening and managementRapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney DiseaseTreatment and Management of Autosomal Dominant Polycystic Kidney DiseaseDifferential Diagnosis of Autosomal Dominant Polycystic Kidney DiseaseThe Treatment of Autosomal Dominant Polycystic Kidney DiseaseAutosomal Dominant Polycystic Kidney Disease Induced by Ciliary DefectsPolycystins and Molecular Basis of Autosomal Dominant Polycystic Kidney DiseaseDiagnostic Imaging of Autosomal Dominant Polycystic Kidney Disease.Seminal Vesicles in Autosomal Dominant Polycystic Kidney DiseaseAutosomal dominant polycystic kidney disease: recent advances in clinical managementNovel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) geneChromosome 4 localization of a second gene for autosomal dominant polycystic kidney diseaseApproaches to testing new treatments in autosomal dominant polycystic kidney disease: insights from the CRISP and HALT-PKD studiesTRPP2 and autosomal dominant polycystic kidney diseaseAutosomal dominant polycystic kidney disease: time for a change?Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease.Urinary proteomic biomarkers for diagnosis and risk stratification of autosomal dominant polycystic kidney disease: a multicentric study
P921
Q54808823-D491FAEE-C5B8-42B5-9A39-9B5498290690Q94219576-D0DA90A5-F7C4-4309-8A83-D7F72A7E15EBQ94219580-CB3F788C-5A47-4360-929D-6FE0EDA097D5Q94219584-F3E428ED-E317-46AC-9DD2-F29CFB51C9CDQ94219588-A0CBB272-ED1F-4447-AF2E-4C70161FF5BEQ94219593-ADDA9595-F612-442C-BD39-0286C44F8701Q94219598-734E82C1-22BB-4E95-A8DC-CD5238326785
P5166
Q22010947-B47203D3-64C7-4330-8760-0D29489C63C4Q22254297-5F6316B5-5175-432C-9D49-BF501338C2DAQ24186484-B13A3040-5F4D-4403-94C7-18F02BF04118Q24201315-6592D62B-F737-4486-8D9E-19CAE135C4AEQ24201920-0D17BF0E-4C64-4B6E-8779-745DF2689C6AQ24290926-2F704B2C-7E1C-4525-8C5A-763D34834E72Q24313458-A423BAA7-5655-437F-9F04-CA0190F92180Q24319147-0C4FF275-8E7C-405F-A471-87C92918AC02Q24320879-FCB24092-9164-429B-BCA2-5E7AA31E168EQ24336734-72ACA031-846E-46AE-9C80-788BD8BC1BD4Q24656249-6C49B5CE-48AC-45DD-8BBD-28BE99A11C4DQ24657714-C340CFAD-2357-4ECE-99C1-06C83F111EBDQ24678335-4B834583-7857-42F4-A4B9-B20B3D1CE5D6Q26767011-85A8F554-3A36-4287-BF89-BC738AA2EB33Q26784073-0B15D300-4F38-4BE6-87D5-692F793135FDQ26798115-1C6B4A86-228D-41E5-A4BC-7339FD835B13Q26799638-BF443C45-4675-43FF-8564-72ED508E1EE4Q26827735-F304E9F9-F46E-48EF-AB3D-B04066E0DCA2Q26862813-3664A0A4-F9E8-4C65-894A-AC6E4289E8E0Q26863397-69363CC1-FEB9-4FCB-A580-02FC7AA005ECQ27000011-6B51626C-E3AC-430B-ACFE-E63F4DE5E4F2Q27007821-9F069A4F-FF97-43E0-B899-E4C0BFD14C95Q27011660-B1540F54-ADF4-4B5E-895A-54984CAE8FF9Q27025388-42734894-9010-4004-8535-0CC191253753Q28066530-2526F8BE-13AA-46FE-BD4C-B990C4CAA50FQ28070261-B20EF0C1-A56E-4DC8-B1F5-7BAF538B1CBDQ28070360-6B439581-F307-49D3-87C0-85D49337B43BQ28077060-D6ABFB6F-F421-48EE-9E03-032770110020Q28078256-6838A2B6-43AD-4947-A643-258C77A8C9BAQ28079571-3D4E7360-93D5-47FE-B340-7C354025CA2BQ28079746-0D102C9B-1695-48FC-968F-413BEADF3000Q28079765-1169FA89-F523-4D1E-9C77-40F67C6C81CAQ28079782-9B8BE4F1-9EE8-4C0C-A3F5-C399EACC2134Q28256830-CA9C8798-7E78-437B-BC68-0A306762DF11Q28259145-ADE060D6-6EE3-4A02-86DE-0FBC0E23C784Q28285181-F8853B6A-E2BB-47B0-85AA-6B2ADC7B8164Q28287644-70A06FF8-3CE2-4E75-A436-EBF9A5BB1CA6Q28297676-94A51F1B-F432-4040-A78C-8907DB2B69E1Q28345772-C731D33E-7579-4857-BD49-2256172C8E22Q28484968-EA9B61B9-D729-449B-9356-D05A81E0E6E1
P921
description
Gruppe ernsthafter, meist erblich bedingter Erkrankungen der Nieren
@de
Sortzetiko gaixotasun bat, zei ...... na eta heriotza eragin ditzake
@eu
congenital disorder of urinary system
@en
disordine genetico di tipo cistico.
@it
genetycznie uwarunkowana choroba nerek
@pl
vrozená vada močové soustavy
@cs
name
Cystenieren
@nl
Wielotorbielowatość nerek
@pl
Zystenniere
@de
autosomal dominant polycystic kidney disease
@en
doença do rim policístico
@pt
kiste anitzeko giltzurrun
@eu
malattia policistica renale
@it
poliquistosi renal
@ca
poliquistosis renal
@es
polycystisk njursjukdom
@sv
type
label
Cystenieren
@nl
Wielotorbielowatość nerek
@pl
Zystenniere
@de
autosomal dominant polycystic kidney disease
@en
doença do rim policístico
@pt
kiste anitzeko giltzurrun
@eu
malattia policistica renale
@it
poliquistosi renal
@ca
poliquistosis renal
@es
polycystisk njursjukdom
@sv
altLabel
Congenital biliary ectasias
@en
PCK - Polycystic kidney disease
@en
POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
@en
Polycystic kidney disease NOS (disorder)
@en
Polycystic kidney disease NOS
@en
Polycystic kidney
@en
Polycystic kidney, unspecified type
@en
giltzurrunetako eritasun polikistiko
@eu
polycystisk nyre
@nn
polycystiske nyrer
@nn
prefLabel
Cystenieren
@nl
Wielotorbielowatość nerek
@pl
Zystenniere
@de
autosomal dominant polycystic kidney disease
@en
doença do rim policístico
@pt
kiste anitzeko giltzurrun
@eu
malattia policistica renale
@it
poliquistosi renal
@ca
poliquistosis renal
@es
polycystisk njursjukdom
@sv
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science/polycystic-renal-disease
P1461
autosomal-dominant-polycystic-kidney-disease
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P1748
P1995
P227
P2892
P373
Polycystic kidney disease
P3827
polycystic-kidney-diseases
P3841
HP:0000113