OMOP Concept 36716029
Hyperuricemia, anemia, renal failure syndrome
StandardConditionSNOMED721840000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hyperuricemia, anemia, renal failure syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 721840000 | Renin associated familial juvenile hyperuricaemic nephropathy | Non-standard |
Synonyms
Alternative names recorded for Hyperuricemia, anemia, renal failure syndrome across source vocabularies.
- Familial juvenile hyperuricaemic nephropathy type 2
- Familial juvenile hyperuricemic nephropathy type 2
- Hyperuricaemia, anaemia, renal failure syndrome
- Hyperuricemia, anemia, renal failure syndrome (disorder)
- Renin associated familial juvenile hyperuricaemic nephropathy
- Renin associated familial juvenile hyperuricemic nephropathy
- síndrome de hiperuricemia, anemia e insuficiencia renal
- síndrome de hiperuricemia, anemia e insuficiencia renal (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(53)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Hereditary nephropathy
- 1Hyperuricemia
- 1Renal tubular disorder
- 1Urate nephropathy
- 2Autosomal hereditary disorder
- 2Blood urate above reference range
- 2Disorder of purine metabolism
- 2Disorder of renal parenchyma
- 2Hereditary disorder of the urinary system
- 2Kidney disease
- 2Metabolic renal disease
- 2Toxic nephropathy
- 3Blood substance level above reference range
- 3Blood urate outside reference range
- 3Disorder of kidney and/or ureter
- 3Disorder of purine and pyrimidine metabolism
- 3Disorder of retroperitoneum
- 3Disorder of urinary system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Kidney finding
- 3Metabolic disease
- 3Uric acid level above reference range
- 4Abdominal organ finding
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