OMOP Concept 4277255
Mannosidosis
StandardConditionSNOMED65524005Disorder
Maps from
5
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Mannosidosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134694 | Mannosidosis | Non-standard |
| MeSH | D044904 | Mannosidase Deficiency Diseases | Non-standard |
| Nebraska Lexicon | 65524005 | Alpha-mannosidase deficiency | Non-standard |
| Read | C31y300 | Mannosidosis | Non-standard |
| Read | C375000 | Mannosidosis | Non-standard |
Synonyms
Alternative names recorded for Mannosidosis across source vocabularies.
- Alpha-D-mannosidosis
- alpha-Mannosidase deficiency
- Alpha-mannosidase deficiency
- deficiencia de alfa manosidasa
- Mannosidosis (disorder)
- manosidosis
- manosidosis (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Dysostosis multiplex group
- 1Hereditary disorder of musculoskeletal system
- 1Oligosaccharidosis
- 2Autosomal hereditary disorder
- 2Congenital anomaly of skeletal bone
- 2Developmental disorder
- 2Disorder of glycoprotein metabolism
- 2Disorder of lysosomal enzyme
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lysosomal storage disease
- 2Metabolic bone disease
- 2Skeletal dysplasia
- 3Congenital anomaly of musculoskeletal system
- 3Congenital disease
- 3Disease
- 3Disorder of body system
- 3Disorder of bone
- 3Disorder of bone development
- 3Disorder of skeletal system
- 3Enzymopathy
- 3Genetic disease
Narrower concepts
(2)Included automatically when you query with descendants.
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