OMOP Concept 35625533
Hypermanganesemia with dystonia
StandardConditionSNOMED768553002Disorder
Maps from
1
Descendants
2
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hypermanganesemia with dystonia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 768553002 | HMNDYT - hypermanganesemia with dystonia | Non-standard |
Synonyms
Alternative names recorded for Hypermanganesemia with dystonia across source vocabularies.
- Familial manganese-induced neurotoxicity
- hipermanganesemia con distonía
- hipermanganesemia con distonía (trastorno)
- HMNDYT - hypermanganesemia with dystonia
- Hypermanganesemia with dystonia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Disorder of manganese metabolism
- 1Dystonia
- 1Hereditary disorder of nervous system
- 2Autosomal hereditary disorder
- 2Disorder of nervous system
- 2Disorder of trace mineral metabolism
- 2Extrapyramidal disease
- 2Hereditary disorder by system
- 3Disorder of body system
- 3Disorder of brain
- 3Disorder of mineral metabolism
- 3Hereditary disease
- 3Movement disorder
- 4Disease
- 4Disorder of head
- 4Disorder of the central nervous system
- 4Finding of brain
- 4Finding of movement
- 4Genetic disease
- 4Metabolic disease
- 5Central nervous system finding
- 5Clinical finding
- 5Head finding
Narrower concepts
(2)Included automatically when you query with descendants.
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