OMOP Concept 36714261
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome
StandardConditionSNOMED719405005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Leukoencephalopathy with metaphyseal chondrodysplasia syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 719405005 | Leukoencephalopathy with metaphyseal chondrodysplasia syndrome | Non-standard |
Synonyms
Alternative names recorded for Leukoencephalopathy with metaphyseal chondrodysplasia syndrome across source vocabularies.
- Leucoencephalopathy with metaphyseal chondrodysplasia syndrome
- Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder)
- síndrome de leucoencefalopatía con condrodisplasia metafisaria
- síndrome de leucoencefalopatía con condrodisplasia metafisaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(48)Roll up to these when you need a wider cohort.
- 1Cerebral degeneration
- 1Developmental hereditary disorder
- 1Hereditary degenerative disease of central nervous system
- 1Hereditary disorder of musculoskeletal system
- 1Leukoencephalopathy
- 1Metaphyseal chondrodysplasia
- 1X-linked recessive hereditary disease
- 2Congenital anomaly of skeletal bone
- 2Congenital malformation syndromes associated with short stature
- 2Degenerative brain disorder
- 2Degenerative disease of the central nervous system
- 2Developmental disorder
- 2Disorder of brain
- 2Disorder of musculoskeletal system
- 2Finding of head region
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary disorder of nervous system
- 2Skeletal dysplasia
- 2X-linked hereditary disease
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation syndrome
- 3Degenerative disorder
- 3Disease
- 3Disorder of body system
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