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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Fanconi Syndrome [Disease/Finding] | |
| Synonyms |
Fanconi Syndrome Proximal Renal Tubular Dysfunction |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001208 |
|
| altLabel |
Fanconi Syndrome Proximal Renal Tubular Dysfunction
|
|
| cui |
C0015624
|
|
| MESH DEFINITION |
A hereditary or acquired form of generalized dysfunction of the PROXIMAL KIDNEY TUBULE without primary involvement of the KIDNEY GLOMERULUS. It is usually characterized by the tubular wasting of nutrients and salts (GLUCOSE; AMINO ACIDS; PHOSPHATES; and BICARBONATES) resulting in HYPOKALEMIA; ACIDOSIS; HYPERCALCIURIA; and PROTEINURIA.
|
|
| MESH DUI |
D005198
|
|
| MeSH name |
Fanconi Syndrome
|
|
| MESH UI |
M0008225
|
|
| NDFRT kind |
DISEASE_KIND
|
|
| notation |
N0000001208
|
|
| NUI |
N0000001208
|
|
| prefLabel |
Fanconi Syndrome [Disease/Finding]
|
|
| SNOMED CID |
40488004 62332007 236466005
|
|
| tui |
T047
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|
| subClassOf |
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