OMOP Concept 4166222
Metachromatic leukodystrophy, late infantile type
StandardConditionSNOMED47683004Disorder
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 Metachromatic leukodystrophy, late infantile type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134256 | Metachromatic leukodystrophy, late infantile type | Non-standard |
| Nebraska Lexicon | 47683004 | Metachromatic leukodystrophy, late infantile type | Non-standard |
Synonyms
Alternative names recorded for Metachromatic leukodystrophy, late infantile type across source vocabularies.
- Greenfield disease
- Late infantile metachromatic leucodystrophy
- leucodistrofia metacromática, tipo infantil tardía
- leucodistrofia metacromática, tipo infantil tardía (trastorno)
- Metachromatic leucodystrophy, late infantile type
- Metachromatic leukodystrophy, late infantile type (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(31)Roll up to these when you need a wider cohort.
- 1Metachromatic leukodystrophy
- 2Autosomal recessive hereditary disorder
- 2Hereditary degenerative disease of central nervous system
- 2Inherited metabolic disorder of nervous system
- 2Leukodystrophy
- 2Sphingolipidosis
- 3Autosomal hereditary disorder
- 3Degenerative disease of the central nervous system
- 3Disorder of lipid storage and metabolism
- 3Hereditary disorder of nervous system
- 3Inborn error of metabolism
- 3Lysosomal storage disease
- 3Neurological lesion
- 3Neuropathy
- 4Clinical finding
- 4Congenital disease
- 4Degenerative disorder
- 4Disorder of lipoprotein AND/OR lipid metabolism
- 4Disorder of nervous system
- 4Disorder of the central nervous system
- 4Enzymopathy
- 4Hereditary disease
- 4Hereditary disorder by system
- 4Hereditary metabolic disease
- 4Storage disease
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