OMOP Concept 4243053
Mucopolysaccharidosis, MPS-III-B
StandardConditionSNOMED59990008Disorder
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-III-B via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133811 | Mucopolysaccharidosis, MPS-III-B | Non-standard |
| Nebraska Lexicon | 59990008 | Mucopolysaccharidosis, MPS-III-B | Non-standard |
Synonyms
Alternative names recorded for Mucopolysaccharidosis, MPS-III-B across source vocabularies.
- alpha-N-acetylglucosaminidase deficiency
- Alpha-N-acetylglucosaminidase deficiency
- deficiencia de alfa - N - acetilglucosaminidasa
- MPS III-B - Mucopolysaccharidosis III-B
- MPSIIIB - Mucopolysaccharidosis type IIIB
- mucopolisacaridosis, MPS - III - B
- mucopolisacaridosis, MPS - III - B (trastorno)
- Mucopolysaccharidosis III-B
- Mucopolysaccharidosis III-B (disorder)
- N-Acetyl-alpha-D-glucosaminidase deficiency
- Sanfilippo syndrome B
- Sanfilippo syndrome, type B
- síndrome de Sanfilippo, tipo B
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Sanfilippo syndrome
- 2Autosomal recessive hereditary disorder
- 2Mucopolysaccharidosis
- 3Autosomal hereditary disorder
- 3Disorder of lysosomal enzyme
- 3Lysosomal storage disease
- 4Congenital disease
- 4Enzymopathy
- 4Hereditary disease
- 4Storage disease
- 5Disorder of fetus and/or newborn
- 5Genetic disease
- 5Inborn error of metabolism
- 5Metabolic disease
- 6Disease
- 6Hereditary metabolic disease
- 7Clinical finding
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