OMOP Concept 4033463
Enamel-renal syndrome
StandardConditionSNOMED109477002Disorder
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 Enamel-renal syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C538241 | Amelogenesis imperfecta nephrocalcinosis | Non-standard |
| Nebraska Lexicon | 109477002 | Amelogenesis imperfecta, nephrocalcinosis and impaired renal concentration | Non-standard |
Synonyms
Alternative names recorded for Enamel-renal syndrome across source vocabularies.
- Amelogenesis imperfecta and nephrocalcinosis
- amelogénesis imperfecta, nefrocalcinosis y defecto en la concentración renal
- amelogénesis imperfecta, nefrocalcinosis y defecto en la concentración renal (trastorno)
- Amelogenesis imperfecta, nephrocalcinosis and impaired renal concentration
- Enamel renal syndrome
- Enamel-renal syndrome (disorder)
- McGibbon Lubinsky syndrome
- síndrome de Lubinsky
- síndrome esmalte - renal
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(77)Roll up to these when you need a wider cohort.
- 1Amelogenesis imperfecta
- 1Autosomal recessive hereditary disorder
- 1Hereditary nephropathy
- 1Nephrocalcinosis
- 1Renal failure syndrome
- 2Autosomal hereditary disorder
- 2Calcinosis
- 2Congenital anomaly of tooth
- 2Developmental hereditary disorder
- 2Disorder of calcium metabolism
- 2Disorder of hard tissues of teeth
- 2Disorder of renal parenchyma
- 2Hereditary disorder of the urinary system
- 2Hereditary disorder of tooth
- 2Kidney disease
- 2Kidney lesion
- 2Metabolic renal disease
- 2Renal impairment
- 3Congenital abnormality of oral cavity
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of jaw
- 3Degenerative disorder
- 3Developmental disorder
- 3Digestive system hereditary disorder
- 3Disorder of kidney and/or ureter
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