OMOP Concept 40479850
Infantile nephronophthisis
StandardConditionSNOMED444558002Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2010
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Infantile nephronophthisis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566582 | Nephronophthisis 2 | Non-standard |
Synonyms
Alternative names recorded for Infantile nephronophthisis across source vocabularies.
- Infantile nephronophthisis (disorder)
- nefronoptisis infantil
- nefronoptisis infantil (trastorno)
- Nephronophthisis type 2
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Nephronophthisis
- 2Autosomal recessive hereditary disorder
- 2Hereditary nephropathy
- 2Nephronophthisis - medullary cystic disease
- 3Autosomal hereditary disorder
- 3Hereditary disorder of the urinary system
- 3Kidney disease
- 3Medullary cystic disease of the kidney
- 4Cyst of kidney
- 4Disorder of kidney and/or ureter
- 4Disorder of retroperitoneum
- 4Disorder of urinary system
- 4Hereditary disease
- 4Hereditary disorder by system
- 4Kidney finding
- 4Renal fibrosis
- 4Structural abnormality of medulla of kidney
- 5Abdominal organ finding
- 5Disorder of abdomen
- 5Disorder of body system
- 5Disorder of renal parenchyma
- 5Disorder of the genitourinary system
- 5Genetic disease
- 5Kidney lesion
- 5Renal mass
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