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Disease Browser
Parent Node:
expandKidney Diseases, Cystic (D052177)
..Starting node
..expandMedullary Sponge Kidney (D007691)

       Child Nodes:
........expandCystic dilatation of renal collecting tubes (C531743)



 Sister Nodes: 
..expandBaraitser Rodeck Garner syndrome (C537906)
..expandBrachymesomelia renal syndrome (C537096)
..expandCerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula (C563731)
..expandCystic Kidney Disease with Ventriculomegaly (C565657)
..expandGlomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria (C563693)
..expandJoubert syndrome 1 (C536293)
..expandJoubert syndrome 2 (C536294)
..expandJoubert syndrome 4 (C536296)
..expandJoubert Syndrome 7 (C566916)
..expandMedullary Sponge Kidney (D007691) Child1
..expandMulticystic Dysplastic Kidney (D021782) Child2
..expandNEPHRONOPHTHISIS 11 (OMIM:613550)
..expandNephronophthisis 2 (C566582)
..expandNephronophthisis 3 (C565780)
..expandNephronophthisis 4 (C564640)
..expandNephronophthisis 7 (C566930)
..expandNephronophthisis, familial juvenile (C537699)
..expandPolycystic Kidney Diseases (D007690) Child21
..expandRenal cysts and diabetes syndrome (C535520)
..expandRENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
..expandSenior Loken Syndrome (C537580)
..expandSenior-Loken Syndrome 3 (C564637)
..expandSenior-Loken syndrome 4 (C537581)
..expandSenior-Loken Syndrome 5 (C563763)
..expandSenior-Loken Syndrome 6 (C565708)
..expandSitus inversus totalis with cystic dysplasia of kidneys and pancreas (C536666)
..expandTsc2 Angiomyolipomas, Renal, Modifier Of (C567682)
..expandUlnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia (C565783)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:6883
Name:Medullary Sponge Kidney
Definition:A non-hereditary KIDNEY disorder characterized by the abnormally dilated (ECTASIA) medullary and inner papillary portions of the collecting ducts. These collecting ducts usually contain CYSTS or DIVERTICULA filled with jelly-like material or small calculi (KIDNEY STONES) leading to infections or obstruction. It should be distinguished from congenital or hereditary POLYCYSTIC KIDNEY DISEASES.
Alternative IDs:
ParentIDs:MESH:D052177
TreeNumbers:C12.777.419.403.500 |C13.351.968.419.403.500
Synonyms:Cacchi Ricci Disease |Cacchi Ricci Syndrome |Cacchi-Ricci Syndrome |Canalicular Ectasia, Precalyceal |Canalicular Ectasias, Precalyceal |Disease, Cacchi Ricci |Ectasia, Precalyceal Canalicular |Ectasias, Precalyceal Canalicular |Kidney, Sponge |Kidneys, Sponge |Me
Slim Mappings:Urogenital disease (female)|Urogenital disease (male)
Reference: MedGen: D007691
MeSH: D007691
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants