OMOP Concept 4029887
Neonatal adrenoleukodystrophy
StandardConditionSNOMED238061001Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Neonatal adrenoleukodystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133425 | Neonatal adrenoleucodystrophy | Non-standard |
| ICD10CM | E71.511 | Neonatal adrenoleukodystrophy | Non-standard |
Synonyms
Alternative names recorded for Neonatal adrenoleukodystrophy across source vocabularies.
- adrenoleucodistrofia del recién nacido
- adrenoleucodistrofia del recién nacido (trastorno)
- Neonatal adrenoleucodystrophy
- Neonatal adrenoleukodystrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Adrenoleukodystrophy
- 1Peroxisome biogenesis disorder
- 2Adrenal cortical hypofunction
- 2Autosomal recessive hereditary disorder
- 2Disorder of peroxisomal function
- 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
- 3Autosomal hereditary disorder
- 3Degenerative disease of the central nervous system
- 3Disorder of adrenal cortex
- 3Disorder of endocrine system
- 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
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