OMOP Concept 35622004
Adrenomyodystrophy
StandardConditionSNOMED763311001Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Adrenomyodystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C538051 | Adrenomyodystrophy | Non-standard |
| Nebraska Lexicon | 763311001 | Adrenomyodystrophy | Non-standard |
Synonyms
Alternative names recorded for Adrenomyodystrophy across source vocabularies.
- adrenomiodistrofia
- adrenomiodistrofia (trastorno)
- Adrenomyodystrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Adrenal cortical hypofunction
- 1Hereditary disorder of endocrine system
- 1X-linked hereditary disease
- 2Disorder of adrenal cortex
- 2Disorder of endocrine system
- 2Hereditary disorder by system
- 2Hypoadrenalism
- 2Sex-linked hereditary disorder
- 3Disorder of adrenal gland
- 3Disorder of body system
- 3Hereditary disease
- 4Abdominal organ finding
- 4Disease
- 4Disorder of retroperitoneum
- 4Genetic disease
- 5Clinical finding
- 5Disorder of abdomen
- 5Finding of abdomen
- 5Viscus structure finding
- 6Disorder of abdominopelvic segment of trunk
- 6Finding of abdominopelvic segment of trunk
- 7Disorder of trunk
- 7Finding of trunk structure
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