OMOP Concept 37117931
Infundibulopelvic stenosis multicystic kidney syndrome
StandardConditionSNOMED725905005Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Infundibulopelvic stenosis multicystic kidney syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535528 | Infundibulopelvic dysgenesis | Non-standard |
| Nebraska Lexicon | 725905005 | Infundibulopelvic stenosis multicystic kidney syndrome | Non-standard |
Synonyms
Alternative names recorded for Infundibulopelvic stenosis multicystic kidney syndrome across source vocabularies.
- Infundibulopelvic dysgenesis
- Infundibulopelvic stenosis multicystic kidney syndrome (disorder)
- síndrome de riñón multiquístico con estenosis infundibulopélvica
- síndrome de riñón multiquístico con estenosis infundibulopélvica (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital anomaly of the kidney
- 1Congenital anomaly of the urinary tract proper
- 1Developmental hereditary disorder
- 1Hereditary nephropathy
- 2Autosomal hereditary disorder
- 2Congenital anomaly of abdomen
- 2Congenital malformation of the urinary system
- 2Developmental disorder
- 2Disorder of urinary tract
- 2Hereditary disease
- 2Hereditary disorder of the urinary system
- 2Kidney disease
- 3Congenital anomaly of lower trunk
- 3Disease
- 3Disorder of abdomen
- 3Disorder of kidney and/or ureter
- 3Disorder of retroperitoneum
- 3Disorder of urinary system
- 3Finding of urinary tract proper
- 3Genetic disease
- 3Genitourinary congenital anomalies
- 3Hereditary disorder by system
- 3Kidney finding
- 4Abdominal organ finding
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