OMOP Concept 4031815
Mucopolysaccharidosis, MPS-IV-B
StandardConditionSNOMED238044004Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Mucopolysaccharidosis, MPS-IV-B via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133807 | Mucopolysaccharidosis, MPS-IV-B | Non-standard |
| ICD10CM | E76.211 | Morquio B mucopolysaccharidoses | Non-standard |
| Nebraska Lexicon | 238044004 | Beta-galactosidase deficiency | Non-standard |
Synonyms
Alternative names recorded for Mucopolysaccharidosis, MPS-IV-B across source vocabularies.
- Morquio B syndrome
- Morquio-like syndrome
- Morquio syndrome B
- MPS IV-B - Mucopolysaccharidosis IV-B
- mucopolisacaridosis tipo IVB
- mucopolisacaridosis, tipo IVB
- mucopolisacaridosis, tipo IVB (trastorno)
- Mucopolysaccharidosis IV-B
- Mucopolysaccharidosis type IVB
- Mucopolysaccharidosis type IVB (disorder)
- síndrome de Morquio B
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.
- 1Morquio syndrome
- 2Autosomal recessive hereditary disorder
- 2Congenital osteodystrophy
- 2Hereditary disorder of musculoskeletal system
- 2Metabolic bone disease
- 2Mucopolysaccharidosis
- 3Autosomal hereditary disorder
- 3Congenital disease
- 3Disorder of bone
- 3Disorder of lysosomal enzyme
- 3Disorder of musculoskeletal system
- 3Hereditary disorder by system
- 3Lysosomal storage disease
- 3Metabolic disease
- 3Osteodystrophy
- 4Bone finding
- 4Degenerative disorder of bone
- 4Disease
- 4Disorder of body system
- 4Disorder of fetus and/or newborn
- 4Disorder of skeletal system
- 4Enzymopathy
- 4Hereditary disease
- 4Musculoskeletal finding
- 4Storage disease
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