OMOP Concept 4238503
Maroteaux-Lamy syndrome, severe form
StandardConditionSNOMED58263000Disorder
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 Maroteaux-Lamy syndrome, severe form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134655 | Maroteaux-Lamy syndrome, severe form | Non-standard |
| Nebraska Lexicon | 58263000 | Maroteaux-Lamy syndrome, severe form | Non-standard |
Synonyms
Alternative names recorded for Maroteaux-Lamy syndrome, severe form across source vocabularies.
- Maroteaux-Lamy syndrome, severe form (disorder)
- síndrome de Maroteaux - Lamy, forma severa
- síndrome de Maroteaux - Lamy, forma severa (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Maroteaux-Lamy syndrome
- 2Autosomal recessive hereditary disorder
- 2Deficiency of N-acetylgalactosamine-4-sulfatase
- 2Developmental hereditary disorder
- 2Mucopolysaccharidosis
- 2Short stature disorder
- 3Autosomal hereditary disorder
- 3Deficiency of cerebroside-sulfatase
- 3Developmental disorder
- 3Disorder of lysosomal enzyme
- 3Disorder of stature
- 3Hereditary disease
- 3Lysosomal storage disease
- 4Congenital disease
- 4Disease
- 4Enzymopathy
- 4Finding of general physiological development
- 4General finding of height
- 4Genetic disease
- 4Inherited metabolic disorder of nervous system
- 4Storage disease
- 5Clinical finding
- 5Disorder of fetus and/or newborn
- 5Height / growth finding
- 5Hereditary disorder of nervous system
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