Bartter syndrome 707742001
SNOMED CT code
| SNOMED code | 707742001 |
|---|---|
| name | Bartter syndrome |
| status | active |
| date introduced | 2015-01-31 |
| fully specified name(s) | Bartter syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Has interpretation | Impaired 260379002 |
| Interprets | Tubular sodium chloride reabsorption function 840727000 |
| attributes - group2 | |
| Finding site | Henle's loop structure 21694000 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Bartter syndrome 707742001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of acid-base balance 26436007 Alkalosis 21420006 Metabolic alkalosis 1388004 Hypokalemic alkalosis 22774003 Bartter syndrome 707742001 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Finding of renal function 1148582006 Renal impairment 236423003 Bartter syndrome 707742001 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Bartter syndrome 707742001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of acid-base balance 26436007 Alkalosis 21420006 Metabolic alkalosis 1388004 Hypochloremic alkalosis 70134007 Bartter syndrome 707742001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of mineral metabolism 45744005 Disorder of phosphate, calcium and vitamin D metabolism 237879001 Disorder of calcium metabolism 71638002 Hypercalciuria 71938000 Bartter syndrome 707742001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Bartter syndrome 707742001 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Disorder of renal parenchyma 767094002 Renal tubular disorder 95568003 Bartter syndrome 707742001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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