OMOP Concept 4219277
Mucopolysaccharidosis, MPS-IV-A
StandardConditionSNOMED7259005Disorder
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 Mucopolysaccharidosis, MPS-IV-A via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133808 | Mucopolysaccharidosis, MPS-IV-A | Non-standard |
| ICD10CM | E76.210 | Morquio A mucopolysaccharidoses | Non-standard |
Synonyms
Alternative names recorded for Mucopolysaccharidosis, MPS-IV-A across source vocabularies.
- Galactosamine-6-sulfatase deficiency
- Galactosamine-6-sulphatase deficiency
- Galactose-6-sulfatase deficiency
- Galactose-6-sulphatase deficiency
- Morquio A syndrome
- Morquio's syndrome, classic form
- Morquio syndrome A
- MPS IV-A-Mucopolysaccharidosis IV-A
- mucopolisacaridosis, MPS - IV - A
- mucopolisacaridosis, MPS - IV - A (trastorno)
- Mucopolysaccharidosis IV-A
- Mucopolysaccharidosis IV-A (disorder)
- N-acetylgalactosamine-6-sulfatase deficiency
- N-acetylgalactosamine-6-sulphatase deficiency
- síndrome de Morquio A
- síndrome de Morquio, forma clásica
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.
- 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 skeletal system
- 4Enzymopathy
- 4Fetal and/or neonatal disorder
- 4Hereditary disease
- 4Musculoskeletal finding
- 4Storage disease
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