OMOP Concept 45757737
Childhood cerebral X-linked adrenoleukodystrophy
StandardConditionSNOMED367041000119108Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2015
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Childhood cerebral X-linked adrenoleukodystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | E71.520 | Childhood cerebral X-linked adrenoleukodystrophy | Non-standard |
Synonyms
Alternative names recorded for Childhood cerebral X-linked adrenoleukodystrophy across source vocabularies.
- adrenoleucodistrofia cerebral ligada al cromosoma X de la infancia
- adrenoleucodistrofia cerebral ligada al cromosoma X de la infancia (trastorno)
- Childhood cerebral X-linked adrenoleucodystrophy
- Childhood cerebral X-linked adrenoleukodystrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Adrenoleukodystrophy
- 2Adrenal cortical hypofunction
- 2Hereditary degenerative disease of central nervous system
- 2Hereditary disorder of endocrine system
- 2Inherited metabolic disorder of nervous system
- 2Leukodystrophy
- 2Loss of single peroxisomal function
- 2X-linked hereditary disease
- 3Degenerative disease of the central nervous system
- 3Disorder of adrenal cortex
- 3Disorder of endocrine system
- 3Disorder of peroxisomal function
- 3Hereditary disorder by system
- 3Hereditary disorder of nervous system
- 3Hypoadrenalism
- 3Inborn error of metabolism
- 3Neurological lesion
- 3Neuropathy
- 3Sex-linked hereditary disorder
- 4Clinical finding
- 4Congenital disease
- 4Degenerative disorder
- 4Disorder of adrenal gland
- 4Disorder of body system
- 4Disorder of nervous system
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