| Descriptor English: | Medullary Sponge Kidney | ||||||
| Descriptor Spanish: |
Riñón Esponjoso Medular
| ||||||
| Descriptor Portuguese: | Rim em Esponja Medular | ||||||
| Descriptor French: | Rein en éponge | ||||||
| Entry term(s): |
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 Medullary Sponge Kidneys Precalyceal Canalicular Ectasia Precalyceal Canalicular Ectasias Ricci Disease, Cacchi Sponge Kidney Sponge Kidney, Medullary Sponge Kidneys Sponge Kidneys, Medullary Syndrome, Cacchi-Ricci |
||||||
| Tree number(s): |
C12.050.351.968.419.403.500 C12.200.777.419.403.500 C12.950.419.403.500 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D007691 | ||||||
| Scope note: | 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. |
||||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||||
| Public MeSH Note: | 2006; see KIDNEY, SPONGE 1965-2005 |
||||||
| History Note: | 2006 (1965) |
||||||
| DeCS ID: | 7860 | ||||||
| Unique ID: | D007691 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1965/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2009/07/06 |
|
|
Medullary Sponge Kidney
- Preferred
| Concept UI |
M0012032 |
| Scope note | 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. |
| Preferred term | Medullary Sponge Kidney |
| Entry term(s) |
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 Medullary Sponge Kidneys Precalyceal Canalicular Ectasia Precalyceal Canalicular Ectasias Ricci Disease, Cacchi Sponge Kidney Sponge Kidney, Medullary Sponge Kidneys Sponge Kidneys, Medullary Syndrome, Cacchi-Ricci |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
