OMOP Concept 374912
Leukodystrophy
StandardConditionSNOMED192781003Disorder
Maps from
7
Descendants
73
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
7 source codes normalize to Leukodystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 116324 | Leukodystrophy | Non-standard |
| HPO | HP_0002415 | Leukodystrophy | Non-standard |
| ICD10CM | G31.80 | Leukodystrophy, unspecified | Non-standard |
| ICD10CM | G93.44 | Adult-onset leukodystrophy with axonal spheroids | Non-standard |
| ICD9CM | 330.0 | Leukodystrophy | Non-standard |
| Read | F100.00 | Leucodystrophy | Non-standard |
| Read | F100z00 | Leucodystrophy NOS | Non-standard |
Synonyms
Alternative names recorded for Leukodystrophy across source vocabularies.
- leucodistrofia
- leucodistrofia (trastorno)
- Leucodystrophy
- Leukodystrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(73)Included automatically when you query with descendants.
- 14H leukodystrophy
- 1Adrenoleukodystrophy
- 1Adult onset autosomal dominant leukodystrophy
- 1Aicardi Goutieres syndrome
- 1Alexander disease
- 1Alkaline ceramidase 3 deficiency
- 1C11ORF73-related autosomal recessive hypomyelinating leukodystrophy
- 1Cholestanol storage disease
- 1Dalmatian leukodystrophy
- 1Dermatoleukodystrophy
- 1Galactosylceramide beta-galactosidase deficiency
- 1HSMN IV
- 1Hypomyelination of early myelinating structures
- 1Hypomyelination with brain stem and spinal cord involvement and leg spasticity
- 1Metachromatic leukodystrophy
- 1MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome
- 1Multiple mitochondrial dysfunctions syndrome type 4
- 1Multiple mitochondrial dysfunctions syndrome type 5
- 1Muscle eye brain disease with bilateral multicystic leukodystrophy
- 1NKX6-2-related autosomal recessive hypomyelinating leukodystrophy
- 1Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy
- 1Pelizaeus-Merzbacher disease
- 1Pelizaeus Merzbacher like disease
- 1Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
- 1RARS-related autosomal recessive hypomyelinating leukodystrophy
Showing 25 of 73. Retrieve the full set via the API.
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