OMOP Concept 608037
Ovarioleukodystrophy
StandardConditionSNOMED1156768008Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2021
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Ovarioleukodystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565836 | Vanishing White Matter Leukodystrophy with Ovarian Failure | Non-standard |
Synonyms
Alternative names recorded for Ovarioleukodystrophy across source vocabularies.
- ovarioleucodistrofia
- ovarioleucodistrofia (trastorno)
- Ovarioleucodystrophy
- Ovarioleukodystrophy (disorder)
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.
- 1Hereditary disorder of endocrine system
- 1Premature ovarian failure
- 1Reproductive system hereditary disorder
- 1Vanishing white matter disease
- 2Autosomal recessive hereditary disorder
- 2Cerebral degeneration
- 2Disorder of endocrine system
- 2Disorder of reproductive system
- 2Hereditary ataxia
- 2Hereditary degenerative disease of central nervous system
- 2Hereditary disorder by system
- 2Leukodystrophy
- 2Leukoencephalopathy
- 2Primary ovarian failure
- 3Ataxia
- 3Autosomal hereditary disorder
- 3Degenerative brain disorder
- 3Degenerative disease of the central nervous system
- 3Disorder of body system
- 3Disorder of brain
- 3Disorder of the genitourinary system
- 3Finding of head region
- 3Hereditary disease
- 3Hereditary disorder of nervous system
- 3Neurological lesion
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