OMOP Concept 4058844
Finnish congenital nephrotic syndrome
StandardConditionSNOMED197601003Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Finnish congenital nephrotic syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 197601003 | Finnish congenital nephrotic syndrome | Non-standard |
| Read | K01w000 | Finnish nephrosis syndrome | Non-standard |
| Read | K01w011 | Microcystic type congenital nephrotic syndrome | Non-standard |
| Read | K01w012 | Congenital Finnish nephrosis | Non-standard |
Synonyms
Alternative names recorded for Finnish congenital nephrotic syndrome across source vocabularies.
- CNF - Finnish congenital nephrotic syndrome
- Congenital Finnish nephrosis
- Finnish congenital nephrotic syndrome (disorder)
- nefrosis congénita tipo finlandesa
- síndrome nefrótico congénito tipo finlandés
- síndrome nefrótico congénito tipo finlandés (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(58)Roll up to these when you need a wider cohort.
- 1Congenital nephrotic syndrome
- 2Autosomal recessive hereditary disorder
- 2Congenital anomaly of the kidney
- 2Developmental hereditary disorder
- 2Hereditary nephropathy
- 2Nephrotic syndrome
- 3Albumin below reference range
- 3Autosomal hereditary disorder
- 3Congenital anomaly of abdomen
- 3Congenital malformation of the urinary system
- 3Developmental disorder
- 3Glomerular disease
- 3Hereditary disease
- 3Hereditary disorder of the urinary system
- 3Kidney disease
- 3Protein-losing nephropathy
- 4Albumin level - finding
- 4Congenital anomaly of lower trunk
- 4Disease
- 4Disorder of abdomen
- 4Disorder of kidney and/or ureter
- 4Disorder of renal parenchyma
- 4Disorder of retroperitoneum
- 4Disorder of urinary system
- 4Genetic disease
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