OMOP Concept 4276356
Adrenoleukodystrophy
StandardConditionSNOMED65389002Disorder
Maps from
9
Descendants
4
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
9 source codes normalize to Adrenoleukodystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 121772 | Adrenal leukodystrophy | Non-standard |
| CIEL | 121773 | Fanconi-Prader Syndrome | Non-standard |
| ICD10CM | E71.52 | X-linked adrenoleukodystrophy | Non-standard |
| ICD10CM | E71.522 | Adrenomyeloneuropathy | Non-standard |
| ICD10CM | E71.528 | Other X-linked adrenoleukodystrophy | Non-standard |
| ICD10CM | E71.529 | X-linked adrenoleukodystrophy, unspecified type | Non-standard |
| MeSH | D000326 | Adrenoleukodystrophy | Non-standard |
| Nebraska Lexicon | 65389002 | Adrenomyeloneuropathy | Non-standard |
| Read | C308200 | X-linked adrenoleucodystrophy | Non-standard |
Synonyms
Alternative names recorded for Adrenoleukodystrophy across source vocabularies.
- adrenoleucodistrofia
- adrenoleucodistrofia ligada al cromosoma X
- adrenoleucodistrofia (trastorno)
- Adrenoleucodystrophy
- Adrenoleukodystrophy (disorder)
- ALD - adrenoleucodistrofia
- ALD - adrenoleukodystrophy
- Bronze Schilder disease
- complejo de Schilder - Addison
- enfermedad de la piel de bronce de Schilder
- enfermedad de Siemerling - Creutzfeldt
- Schilder-Addison complex
- Siemerling-Creutzfeldt disease
- X-linked adrenoleucodystrophy
- X-linked adrenoleukodystrophy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Adrenal cortical hypofunction
- 1Hereditary degenerative disease of central nervous system
- 1Hereditary disorder of endocrine system
- 1Inherited metabolic disorder of nervous system
- 1Leukodystrophy
- 1Loss of single peroxisomal function
- 1X-linked hereditary disease
- 2Degenerative disease of the central nervous system
- 2Disorder of adrenal cortex
- 2Disorder of endocrine system
- 2Disorder of peroxisomal function
- 2Hereditary disorder by system
- 2Hereditary disorder of nervous system
- 2Hypoadrenalism
- 2Inborn error of metabolism
- 2Neurological lesion
- 2Neuropathy
- 2Sex-linked hereditary disorder
- 3Clinical finding
- 3Congenital disease
- 3Degenerative disorder
- 3Disorder of adrenal gland
- 3Disorder of body system
- 3Disorder of nervous system
- 3Disorder of the central nervous system
Narrower concepts
(4)Included automatically when you query with descendants.
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