Hyperuricemia, anemia, renal failure syndrome 721840000
SNOMED CT code
| SNOMED code | 721840000 |
|---|---|
| name | Hyperuricemia, anemia, renal failure syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Hyperuricemia, anemia, renal failure syndrome (disorder) |
| synonyms |
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| attributes - group1 | |
| Causative agent | Urate 88476001 |
| Finding site | Renal tubule structure 58471003 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Hyperuricemia, anemia, renal failure syndrome 721840000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Urate nephropathy 236495001 Hyperuricemia, anemia, renal failure syndrome 721840000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of purine and pyrimidine metabolism 238006008 Disorder of purine metabolism 32612005 Hyperuricemia 35885006 Hyperuricemia, anemia, renal failure syndrome 721840000 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Hyperuricemia, anemia, renal failure syndrome 721840000 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 Hyperuricemia, anemia, renal failure syndrome 721840000 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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