OMOP Concept 4126106
Specific renal tubule transport defect
StandardConditionSNOMED236470002Disorder
Maps from
1
Descendants
32
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Specific renal tubule transport defect via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Read | K08yG00 | Specific renal tubule transport defect | Non-standard |
Synonyms
Alternative names recorded for Specific renal tubule transport defect across source vocabularies.
- defecto de transporte específico del túbulo renal
- defecto de transporte específico del túbulo renal (trastorno)
- Specific renal tubule transport defect (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Kidney disease
- 2Disorder of kidney and/or ureter
- 2Disorder of retroperitoneum
- 2Kidney finding
- 3Abdominal organ finding
- 3Disorder of abdomen
- 3Disorder of urinary system
- 3Urinary system finding
- 4Disorder of abdominopelvic segment of trunk
- 4Disorder of the genitourinary system
- 4Finding of abdomen
- 4Urogenital finding
- 4Viscus structure finding
- 5Clinical finding
- 5Disorder of body system
- 5Disorder of trunk
- 5Finding of abdominopelvic segment of trunk
- 6Disease
- 6Finding of trunk structure
Narrower concepts
(32)Included automatically when you query with descendants.
- 1Cystinuria
- 1Dibasic aminoaciduria
- 1Familial hypokalemic alkalosis, Gullner type
- 1Familial methionine malabsorption
- 1Familial renal hypouricemia
- 1Glycinuria
- 1High renal threshold for glucose
- 1Histidine transport defect
- 1Iminoglycinuria
- 1Isolated hypercystinuria
- 1Neutral 1 amino acid transport defect
- 1Renal glycosuria
- 2Cystinuria, type 1
- 2Cystinuria, type 2
- 2Cystinuria, type 3
- 2Dibasic amino aciduria type 1
- 2Familial renal glucosuria
- 2Familial renal iminoglycinuria
- 2Hartnup disorder, renal/jejunal type
- 2Hartnup disorder, renal type
- 2Isolated cystinuria
- 2Low renal threshold for glucose
- 2Lysinuric protein intolerance
- 2Neonatal iminoglycinuria
- 2Pregnancy-related glycosuria
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