OMOP Concept 4074393
Primary hyperoxaluria
StandardConditionSNOMED17901006Disorder
Maps from
6
Descendants
4
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
6 source codes normalize to Primary hyperoxaluria via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 129116 | Primary hyperoxaluria | Non-standard |
| ICD10CM | E72.53 | Primary hyperoxaluria | Non-standard |
| ICD10CM | E72.538 | Other specified primary hyperoxaluria | Non-standard |
| ICD10CM | E72.539 | Primary hyperoxaluria, unspecified | Non-standard |
| MeSH | D006960 | Hyperoxaluria, Primary | Non-standard |
| OXMIS | 2718A | HYPEROXALURIA PRIMARY | Non-standard |
Synonyms
Alternative names recorded for Primary hyperoxaluria across source vocabularies.
- hiperoxaluria primaria
- hiperoxaluria primaria (trastorno)
- oxalosis primaria
- Primary hyperoxaluria (disorder)
- Primary oxalosis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(35)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Disorder of carbohydrate metabolism
- 1Enzymopathy
- 1Hereditary nephropathy
- 1Hyperoxaluria
- 1Inborn error of metabolism
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Hereditary disorder of the urinary system
- 2Hereditary metabolic disease
- 2Kidney disease
- 2Metabolic disease
- 2Metabolic renal disease
- 3Disease
- 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
- 4Abdominal organ finding
- 4Clinical finding
- 4Disorder of abdomen
- 4Disorder of body system
Showing 25 of 35. Retrieve the full set via the API.
Narrower concepts
(4)Included automatically when you query with descendants.
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