OMOP Concept 4172011
Congenital nephrotic syndrome
StandardConditionSNOMED48796009Disorder
Maps from
5
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
5 source codes normalize to Congenital nephrotic syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143811 | Congenital nephrotic syndrome | Non-standard |
| HPO | HP_0008677 | Congenital nephrotic syndrome | Non-standard |
| MeSH | C535761 | Nephrosis, congenital | Non-standard |
| Read | K01w.00 | Congenital nephrotic syndrome | Non-standard |
| Read | K01wz00 | Congenital nephrotic syndrome NOS | Non-standard |
Synonyms
Alternative names recorded for Congenital nephrotic syndrome across source vocabularies.
- Congenital nephrotic syndrome (disorder)
- Familial nephrotic syndrome
- síndrome nefrótico congénito
- síndrome nefrótico congénito (trastorno)
- síndrome nefrótico familiar
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(61)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of the kidney
- 1Developmental hereditary disorder
- 1Genetic disease of glomerulus
- 1Hereditary nephropathy
- 1Nephrotic syndrome
- 1Structural abnormality of renal corpuscle
- 2Albumin below reference range
- 2Autosomal hereditary disorder
- 2Congenital anomaly of abdomen
- 2Congenital malformation of the urinary system
- 2Developmental disorder
- 2Genetic disease
- 2Glomerular disease
- 2Hereditary disease
- 2Hereditary disorder of the urinary system
- 2Kidney disease
- 2Protein-losing nephropathy
- 2Structural abnormality of nephron
- 3Albumin level - finding
- 3Congenital anomaly of lower trunk
- 3Disease
- 3Disorder of abdomen
- 3Disorder of kidney and/or ureter
- 3Disorder of renal parenchyma
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Narrower concepts
(2)Included automatically when you query with descendants.
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