OMOP Concept 4107302
Neonatal iminoglycinuria
StandardConditionSNOMED25765006Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Neonatal iminoglycinuria via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133395 | Neonatal Iminoglycinuria | Non-standard |
| Nebraska Lexicon | 25765006 | Neonatal iminoglycinuria | Non-standard |
Synonyms
Alternative names recorded for Neonatal iminoglycinuria across source vocabularies.
- iminoglicinuria neonatal
- iminoglicinuria neonatal (trastorno)
- Neonatal iminoglycinuria (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Iminoglycinuria
- 1Neonatal metabolic disorder
- 1Neonatal renal disorder
- 2Amino acid transport disorder
- 2Kidney disease
- 2Metabolic disease
- 2Metabolic renal disease
- 2Neonatal disorder
- 2Specific renal tubule transport defect
- 3Disease
- 3Disorder of amino acid and organic acid metabolism
- 3Disorder of fetus and/or newborn
- 3Disorder of kidney and/or ureter
- 3Disorder of retroperitoneum
- 3Finding of neonate
- 3Kidney finding
- 3Metabolic disorder of transport
- 4Abdominal organ finding
- 4Clinical finding
- 4Disorder of abdomen
- 4Disorder of amino acid metabolism
- 4Disorder of urinary system
- 4Urinary system finding
- 5Disorder of abdominopelvic segment of trunk
- 5Disorder of organic acid metabolism
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