OMOP Concept 4124551
Lysinuric protein intolerance
StandardConditionSNOMED303852004Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
5 source codes normalize to Lysinuric protein intolerance via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 135441 | Lysinuric Protein Intolerance, Type 2 | Non-standard |
| CIEL | 135443 | Lysinuric protein intolerance | Non-standard |
| MeSH | C562687 | Lysinuric Protein Intolerance | Non-standard |
| Read | C300C00 | Lysinuric protein intolerance | Non-standard |
| Read | C300C11 | Dibasic aminoaciduria - type II | Non-standard |
Synonyms
Alternative names recorded for Lysinuric protein intolerance across source vocabularies.
- aminoaciduria dibásica II
- aminoaciduria hiperdibásica
- Congenital lysinuria
- Dibasic amino aciduria II
- Hyperdibasic aminoaciduria
- intolerancia proteica lisinúrica
- intolerancia proteica lisinúrica (trastorno)
- lisinuria congénita
- LPI - Lysinuric protein intolerance
- Lysinuric protein intolerance (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(39)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Dibasic aminoaciduria
- 1Hereditary nephropathy
- 1Inborn error of metabolism
- 2Amino acid transport disorder
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Genetic disease
- 2Hereditary disorder of the urinary system
- 2Hereditary metabolic disease
- 2Kidney disease
- 2Metabolic renal disease
- 2Specific renal tubule transport defect
- 3Disease
- 3Disorder of amino acid and organic acid metabolism
- 3Disorder of kidney and/or ureter
- 3Disorder of retroperitoneum
- 3Disorder of urinary system
- 3Fetal and/or neonatal disorder
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Kidney finding
- 3Metabolic disease
- 3Metabolic disorder of transport
- 4Abdominal organ finding
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