OMOP Concept 37109814
Sialidosis type 1
StandardConditionSNOMED723675006Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
1 source code normalizes to Sialidosis type 1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 132671 | Normosomatic sialidosis | Non-standard |
Synonyms
Alternative names recorded for Sialidosis type 1 across source vocabularies.
- Cherry red spot myoclonus syndrome
- Lipomucopolysaccharidosis
- Normomorphic sialidosis
- sialidosis tipo 1
- sialidosis tipo 1 (trastorno)
- Sialidosis type 1 (disorder)
- síndrome de mancha rojo cereza y mioclonía
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(27)Roll up to these when you need a wider cohort.
- 1Sialidosis
- 2Autosomal recessive hereditary disorder
- 2Inherited metabolic disorder of nervous system
- 2Mucolipidosis
- 2Myoclonic disorder
- 2Oligosaccharidosis
- 3Autosomal hereditary disorder
- 3Disorder of glycoprotein metabolism
- 3Disorder of lysosomal enzyme
- 3Disorder of nervous system
- 3Hereditary disorder of nervous system
- 3Inborn error of metabolism
- 3Lysosomal storage disease
- 3Movement disorder
- 4Congenital disease
- 4Disease
- 4Disorder of body system
- 4Enzymopathy
- 4Finding of movement
- 4Hereditary disease
- 4Hereditary disorder by system
- 4Hereditary metabolic disease
- 4Storage disease
- 5Clinical finding
- 5Fetal and/or neonatal disorder
Showing 25 of 27. Retrieve the full set via the API.
Get this concept via the API
Resolve Sialidosis type 1 - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/37109814?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card