OMOP Concept 36713457
Bartter syndrome type 4a
StandardConditionSNOMED717791000Disorder
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 Bartter syndrome type 4a via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566530 | Bartter Syndrome, Type 4A | Non-standard |
Synonyms
Alternative names recorded for Bartter syndrome type 4a across source vocabularies.
- Bartter syndrome type 4a (disorder)
- síndrome de Bartter tipo 4a
- síndrome de Bartter tipo 4a (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(76)Roll up to these when you need a wider cohort.
- 1Bartter syndrome type 4
- 2Bartter syndrome
- 2Congenital sensorineural hearing loss
- 2Hereditary hearing loss
- 3Auditory system hereditary disorder
- 3Autosomal recessive hereditary disorder
- 3Congenital hearing disorder
- 3Hearing loss
- 3Hereditary nephropathy
- 3Hypercalciuria
- 3Hypochloremic alkalosis
- 3Hypokalemic alkalosis
- 3Metabolic renal disease
- 3Renal impairment
- 3Renal tubular disorder
- 3Sensorineural hearing loss
- 4Autosomal hereditary disorder
- 4Congenital disease
- 4Disorder of auditory system
- 4Disorder of calcium metabolism
- 4Disorder of renal parenchyma
- 4Disorder of urinary system
- 4Finding of renal function
- 4Hearing disorder
- 4Hereditary disorder by system
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