OMOP Concept 45763665
Bartter syndrome type 3
StandardConditionSNOMED700111000Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Bartter syndrome type 3 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537653 | Bartter syndrome, type 3 | Non-standard |
Synonyms
Alternative names recorded for Bartter syndrome type 3 across source vocabularies.
- Bartter's syndrome type 3
- Bartter syndrome type 3 (disorder)
- Classic Bartter syndrome
- síndrome de Bartter, tipo 3
- síndrome de Bartter, tipo 3 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(63)Roll up to these when you need a wider cohort.
- 1Bartter syndrome
- 2Autosomal recessive hereditary disorder
- 2Hereditary nephropathy
- 2Hypercalciuria
- 2Hypochloremic alkalosis
- 2Hypokalemic alkalosis
- 2Metabolic renal disease
- 2Renal impairment
- 2Renal tubular disorder
- 3Autosomal hereditary disorder
- 3Disorder of calcium metabolism
- 3Disorder of renal parenchyma
- 3Disorder of urinary system
- 3Finding of renal function
- 3Hereditary disorder of the urinary system
- 3Hypokalemia
- 3Impaired urinary system function
- 3Kidney disease
- 3Metabolic alkalosis
- 3Metabolic disease
- 3Urine calcium above reference range
- 4Alkalosis
- 4Disease
- 4Disorder of kidney and/or ureter
- 4Disorder of phosphate, calcium and vitamin D metabolism
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