OMOP Concept 45765442
Hypomyelination and congenital cataract
StandardConditionSNOMED702379005Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2014
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
2 source codes normalize to Hypomyelination and congenital cataract via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C567166 | Leukodystrophy, Hypomyelinating, 5 | Non-standard |
| Nebraska Lexicon | 702379005 | Hypomyelination and congenital cataract | Non-standard |
Synonyms
Alternative names recorded for Hypomyelination and congenital cataract across source vocabularies.
- HCC - hypomyelination and congenital cataract
- hipomielinización y catarata congénita
- hipomielinización y catarata congénita (trastorno)
- Hypomyelination and congenital cataract (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Hereditary disorder of nervous system
- 1Leukoencephalopathy
- 2Autosomal hereditary disorder
- 2Disorder of brain
- 2Disorder of nervous system
- 2Finding of head region
- 2Hereditary disorder by system
- 3Disorder of body system
- 3Disorder of head
- 3Disorder of the central nervous system
- 3Finding of brain
- 3Head finding
- 3Hereditary disease
- 4Central nervous system finding
- 4Clinical finding
- 4Disease
- 4Genetic disease
Get this concept via the API
Resolve Hypomyelination and congenital cataract - 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/45765442?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card