OMOP Concept 4305572
Spondyloenchondromatosis with basal ganglia calcification
StandardConditionSNOMED389271000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Spondyloenchondromatosis with basal ganglia calcification via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 389271000 | Spondyloenchondromatosis with basal ganglia calcification | Non-standard |
Synonyms
Alternative names recorded for Spondyloenchondromatosis with basal ganglia calcification across source vocabularies.
- espondiloencondromatosis con calcificación de ganglios basales
- espondiloencondromatosis con calcificación de ganglios basales (trastorno)
- Spondyloenchondromatosis with basal ganglia calcification (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Disorder of basal ganglia
- 1Hereditary disorder of nervous system
- 1Spondyloenchondromatosis
- 2Autosomal recessive hereditary disorder
- 2Connective tissue hereditary disorder
- 2Developmental hereditary disorder
- 2Disorder of brain
- 2Disorder of nervous system
- 2Disorganized development of cartilaginous and fibrous components of the skeleton
- 2Finding of head region
- 2Hereditary disorder by system
- 2Hereditary disorder of musculoskeletal system
- 3Autosomal hereditary disorder
- 3Congenital anomaly of cartilage
- 3Developmental disorder
- 3Disorder of body system
- 3Disorder of connective tissue
- 3Disorder of head
- 3Disorder of musculoskeletal system
- 3Disorder of the central nervous system
- 3Finding of brain
- 3Head finding
- 3Hereditary disease
- 3Skeletal dysplasia
- 4Cartilage disorder
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