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Cystic kidney disease refers to a wide range of hereditary, developmental, and acquired conditions and with the inclusion of neoplasms with cystic changes, over 40 classifications and subtypes have been identified. Depending on the disease classification, the presentation may be at birth, or much later into adult life. Cystic disease may involve one or both kidneys and may, or may not, occur in the presence of other anomalies. A higher incidence is found in males and prevalence increases with age. Renal cysts have been reported in more than 50% of patients over the age of 50. Typically, cysts grow up to 2.88 mm annually and may cause related pain and/or hemorrhage.

AttributesValues
rdf:type
rdfs:label
  • Cystic kidney disease (en)
  • 嚢胞性腎疾患 (ja)
rdfs:comment
  • 嚢胞性腎疾患(英: cystic kidney disease)とは嚢胞性の腎疾患の一群の総称である。多くの症候群からなるが多発性嚢胞腎(en:Polycystic kidney disease)としては常染色体優性多発性嚢胞腎（ADPKD）、常染色体劣性遺伝をする多発性腎嚢胞（ARPKD）に分類される。ARPKDは小児の稀な疾患である。その他の疾患としては結節性硬化症、von Hippel-Lindau病などの先天性疾患や単純性腎嚢胞、多嚢胞化腎萎縮、(en:Medullary sponge kidney)などがあげられる。 (ja)
  • Cystic kidney disease refers to a wide range of hereditary, developmental, and acquired conditions and with the inclusion of neoplasms with cystic changes, over 40 classifications and subtypes have been identified. Depending on the disease classification, the presentation may be at birth, or much later into adult life. Cystic disease may involve one or both kidneys and may, or may not, occur in the presence of other anomalies. A higher incidence is found in males and prevalence increases with age. Renal cysts have been reported in more than 50% of patients over the age of 50. Typically, cysts grow up to 2.88 mm annually and may cause related pain and/or hemorrhage. (en)
foaf:name
  • Cystic kidney disease (en)
name
  • Cystic kidney disease (en)
foaf:depiction
  • http://commons.wikimedia.org/wiki/Special:FilePath/Autosomal_Dominant_Polycystic_Kidney_Disease.svg
  • http://commons.wikimedia.org/wiki/Special:FilePath/Autosomal_recessive_polycystic_kidney_disease.svg
  • http://commons.wikimedia.org/wiki/Special:FilePath/Cystic_dysplastic_kidney.svg
  • http://commons.wikimedia.org/wiki/Special:FilePath/Grade_5_Vesico_Ureteric_Reflux.svg
  • http://commons.wikimedia.org/wiki/Special:FilePath/Multicystic_Dysplastic_kidney.svg
  • http://commons.wikimedia.org/wiki/Special:FilePath/Posterior_Urethral_Valve.svg
  • http://commons.wikimedia.org/wiki/Special:FilePath/Severe_pelvi-ureteric_junction_obstruction.svg
  • http://commons.wikimedia.org/wiki/Special:FilePath/Simple_renal_cyst.jpg
dcterms:subject
Wikipage page ID
Wikipage revision ID
Link from a Wikipage to another Wikipage
sameAs
SNOMED CT
dbp:wikiPageUsesTemplate
thumbnail
ICD
MeshID
  • D052177 (en)
caption
  • Renal cyst (en)
has abstract
  • Cystic kidney disease refers to a wide range of hereditary, developmental, and acquired conditions and with the inclusion of neoplasms with cystic changes, over 40 classifications and subtypes have been identified. Depending on the disease classification, the presentation may be at birth, or much later into adult life. Cystic disease may involve one or both kidneys and may, or may not, occur in the presence of other anomalies. A higher incidence is found in males and prevalence increases with age. Renal cysts have been reported in more than 50% of patients over the age of 50. Typically, cysts grow up to 2.88 mm annually and may cause related pain and/or hemorrhage. Of the cystic kidney diseases, the most common is polycystic kidney disease with two sub-types: the less prevalent autosomal recessive and more prevalent autosomal dominant. Autosomal recessive polycystic kidney disease (ARPKD) is primarily diagnosed in infants and young children while autosomal dominant polycystic kidney disease (ADPKD) is most often diagnosed in adulthood. Another example of cystic kidney disease is Medullary sponge kidney. (en)
  • 嚢胞性腎疾患(英: cystic kidney disease)とは嚢胞性の腎疾患の一群の総称である。多くの症候群からなるが多発性嚢胞腎(en:Polycystic kidney disease)としては常染色体優性多発性嚢胞腎（ADPKD）、常染色体劣性遺伝をする多発性腎嚢胞（ARPKD）に分類される。ARPKDは小児の稀な疾患である。その他の疾患としては結節性硬化症、von Hippel-Lindau病などの先天性疾患や単純性腎嚢胞、多嚢胞化腎萎縮、(en:Medullary sponge kidney)などがあげられる。 (ja)
eMedicineSubj
  • med (en)
eMedicineTopic
ICD9
  • 753.1
eMedicine subject
  • med (en)
eMedicine topic
  • 3189 (en)
MeSH ID
  • D052177
prov:wasDerivedFrom
page length (characters) of wiki page
ICD10
  • Q61.
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