OMOP Concept 4044058
Autosomal dominant late onset basal ganglia degeneration
StandardConditionSNOMED230313001Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant late onset basal ganglia degeneration via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Read | F13z600 | Neuroferritinopathy | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant late onset basal ganglia degeneration across source vocabularies.
- Autosomal dominant late onset basal ganglia degeneration (disorder)
- degeneración autosómica dominante de los ganglios basales de inicio tardío
- degeneración autosómica dominante de los ganglios basales de inicio tardío (trastorno)
- Neuroferritinopathy
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 dominant hereditary disorder
- 1Basal ganglia degeneration with calcification
- 1Hereditary degenerative disease of central nervous system
- 2Autosomal hereditary disorder
- 2Calcification of basal ganglia
- 2Chorea
- 2Degenerative disease of the central nervous system
- 2Hereditary disorder of nervous system
- 3Cerebral calcification
- 3Degenerative disorder
- 3Disorder of basal ganglia
- 3Disorder of nervous system
- 3Disorder of the central nervous system
- 3Extrapyramidal disease
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Involuntary movement
- 4Calcinosis
- 4Central nervous system finding
- 4Cerebral degeneration
- 4Disease
- 4Disorder of body system
- 4Disorder of brain
- 4Finding of head region
- 4Finding of movement
Showing 25 of 34. Retrieve the full set via the API.
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