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1,534 Possible Causes for Cystic Kidney Disease

  • Cystic Kidney

    SUMMARY: At present, there are no specific treatments available for patients with cystic kidney disease.[ncbi.nlm.nih.gov] Abstract Cystic kidney disease is an important cause of chronic renal failure.[ncbi.nlm.nih.gov] Almost all of proteins associated with a broad spectrum of human cystic kidney diseases have been localized to the region in or around the cilia.[ncbi.nlm.nih.gov]

  • Solitary Renal Cyst

    Over the past two decades, endoscopic surgery for cystic kidney disease minimize surgical trauma so that they became comparable to puncture techniques, and surpass them in[kazan-medjournal.ru] NIH: National Institute of Diabetes and Digestive and Kidney Diseases Acquired Cystic Kidney Disease - NIH (National Institute of Diabetes and Digestive and Kidney Diseases[icdlist.com] kidney, adult type Q61.3 Polycystic kidney, unspecified Q61.4 Renal dysplasia Q61.5 Medullary cystic kidney Q61.8 Other cystic kidney diseases Q61.9 Cystic kidney disease,[icd10data.com]

  • Familial Interstitial Nephritis

    cystic kidney disease 2 familial juvenile hyperuricaemic nephropathy uromodulin chromosome 16p gout Medullary cystic kidney disease 2 (MCKD2) 1 and familial juvenile hyperuricaemic[jmg.bmj.com] Medullary Cystic Kidney Disease. In: NORD Guide to Rare Disorders. Lippincott Williams & Wilkins. Philadelphia, PA. 2003:693-94. Bleyer AJ.[rarediseases.org] Autosomal-dominant medullary cystic kidney disease type 1: clinical and molecular findings in six large Cypriot families. Kidney Int 2002;62(4):1385-94.[revistanefrologia.com]

  • Renal Cysts and Diabetes Syndrome

    2012 ICD-9-CM Diagnosis Code 753.19 Other specified cystic kidney disease Short description: Cystic kidney diseas NEC.[icd9data.com] Unlike other cystic kidney diseases, the tubules in GCKD usually remain unaffected.[renalandurologynews.com] NIH: National Institute of Diabetes and Digestive and Kidney Diseases Acquired Cystic Kidney Disease - NIH (National Institute of Diabetes and Digestive and Kidney Diseases[icdlist.com]

  • Zellweger Syndrome

    kidney disease:常染色体劣性多嚢胞の腎臓疾患 Congenital disorder of glycosylation type 1A:CDG症候群 IA型 Congenital disorder of glycosylation type 1E:CDG症候群 IE型 Nonsyndromic hearing loss and[mondomedi.com] Autosomal recessive inheritance常染色体劣性遺伝 Spinal muscular atrophy:脊髄性筋萎縮症 Cystic fibrosis:嚢胞性線維症 Beta thalassemia:βサラセミア Sickle cell anemia:鎌状赤血球貧血 Autosomal recessive polycystic[mondomedi.com]

  • Polycystic Kidney Disease

    Summary At present, there are no specific treatments available for patients with cystic kidney disease.[doi.org] These proteins, and many others associated with cystic kidney disease, localize to primary cilia, which may act as flow sensors in the kidney; cystic kidney diseases have[ncbi.nlm.nih.gov] Cystic Kidney Disease Types Primary PKD Autosomal dominant PKD PKD type 1 PKD type 2 Autosomal recessive PKD Secondary Cystic Kidney Disease Aquired cystic kidney disease[healthcommunities.com]

  • Patau Syndrome

    Please log in to edit this article. Edit Synonym: Trisomy 13, Bartholin-Patau-Syndrome German : Trisomie 13, Pätau-Syndrom 1 Definition The Patau syndrome, also known as trisomy 13, is a malformation syndrome that is caused by a numerical chromosome aberration. A separation error during the meiosis leads to there[…][flexikon.doccheck.com]

  • Fabry Disease

    Enzyme replacement therapy (ERT) for Fabry disease does not show a clear benefit in angiokeratoma. We describe two Japanese siblings with Fabry disease, who were diagnosed when angiokeratomas were found on the older sibling at the age of 13 years. Neither of the boys complained of pain, while both suffered from[…][ncbi.nlm.nih.gov]

  • Autosomal Dominant Polycystic Kidney Disease

    2015 ICD-9-CM Diagnosis Code 753.1 Cystic kidney disease There are 9 ICD-9-CM codes below 753.1 that define this diagnosis in greater detail.[icd9data.com] Autosomal dominant polycystic kidney disease is one of the most prevalent forms of inherited cystic kidney disease, and can be characterized by kidney cyst formation and enlargement[ncbi.nlm.nih.gov] BACKGROUND/AIMS: Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common inherited cystic kidney diseases caused by mutations in two large multi-exon[ncbi.nlm.nih.gov]

  • Bilateral Multicystic Dysplastic Kidney

    Q61.8 Other cystic kidney diseases Q61.9 Cystic kidney disease, unspecified Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter Q62.0[icd10data.com] NIH: National Institute of Diabetes and Digestive and Kidney Diseases Acquired Cystic Kidney Disease - NIH (National Institute of Diabetes and Digestive and Kidney Diseases[icdlist.com] Other cystic kidney diseases can include the following: * Autosomal recessive and, less commonly, autosomal dominant polycystic kidney disease. * Familial juvenile nephronophthisis[medhelp.org]

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