OMOP Concept 374912
Leukodystrophy
StandardConditionSNOMED192781003Disorder
Maps from
9
Descendants
74
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
9 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 |
| Nebraska Lexicon | 192781003 | Leucodystrophy | Non-standard |
| Nebraska Lexicon | 307360006 | Leucodystrophy without a known biochemical basis | 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
(74)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
- 1Cavitating leukodystrophy
- 1Cholestanol storage disease
- 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
- 1Neuroaxonal 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
- 1RAVINE syndrome
- 1RNA polymerase III-related leukodystrophy
- 1Spongy degeneration of central nervous system
- 1TUBB4A-related leukodystrophy
- 1Vanishing white matter disease
- 1VPS11-related autosomal recessive hypomyelinating leukodystrophy
- 1X-linked spastic paraplegia type 2
- 2Adolescent X-linked adrenoleukodystrophy
- 2Adrenomyeloneuropathy
- 2Aicardi Goutieres syndrome type 1
- 2Aicardi Goutieres syndrome type 2
- 2Aicardi Goutieres syndrome type 3
- 2Aicardi Goutieres syndrome type 4
- 2Aicardi Goutieres syndrome type 5
- 2Alexander disease type I
- 2Alexander disease type II
- 2Arylsulfatase A deficiency
- 2Ataxia co-occurrent and due to phytanic acid storage disease
- 2Childhood cerebral X-linked adrenoleukodystrophy
- 2Dystonia due to metachromatic leucodystrophy
- 2Galactocerebroside beta-galactosidase deficiency - early onset
- 2Globoid cell leukodystrophy, late-onset
- 2Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
- 2Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome
Get this concept via the API
Resolve Leukodystrophy - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/374912?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card