OMOP Concept 36716448
Juvenile cataract, microcornea, renal glucosuria syndrome
StandardConditionSNOMED722457005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Juvenile cataract, microcornea, renal glucosuria syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 722457005 | Juvenile cataract, microcornea, renal glucosuria syndrome | Non-standard |
Synonyms
Alternative names recorded for Juvenile cataract, microcornea, renal glucosuria syndrome across source vocabularies.
- Juvenile cataract, microcornea, renal glucosuria syndrome (disorder)
- síndrome de catarata juvenil, microcórnea y glucosuria renal
- síndrome de catarata juvenil, microcórnea y glucosuria renal (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(68)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Disorder of carbohydrate absorption
- 1Familial renal glucosuria
- 1Hereditary disorder of the visual system
- 1Hereditary nephropathy
- 1Juvenile cataract
- 1Metabolic renal disease
- 1Microcornea
- 2Autosomal hereditary disorder
- 2Congenital structural abnormality of cornea
- 2Developmental disorder
- 2Disorder of carbohydrate metabolism
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary disorder of the urinary system
- 2Infantile and/or juvenile cataract
- 2Kidney disease
- 2Metabolic disease
- 2Renal glycosuria
- 2Visual system disorder
- 3Cataract
- 3Congenital anomaly of anterior segment of eye
- 3Disease
- 3Disorder of body system
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