OMOP Concept 36714027
Autosomal recessive spastic paraplegia type 39
StandardConditionSNOMED719103009Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Autosomal recessive spastic paraplegia type 39 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C567433 | Spastic Paraplegia 39, Autosomal Recessive | Non-standard |
| Nebraska Lexicon | 719103009 | Spastic paraplegia due to neuropathy target esterase mutation | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive spastic paraplegia type 39 across source vocabularies.
- Autosomal recessive spastic paraplegia type 39 (disorder)
- paraplejía espástica autosómica recesiva tipo 39
- paraplejía espástica autosómica recesiva tipo 39 (trastorno)
- Spastic paraplegia due to neuropathy target esterase mutation
- Spastic paraplegia due to NTE (neuropathy target esterase) mutation
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(46)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary spastic paraplegia
- 1Complicated hereditary spastic paraplegia
- 2Autosomal recessive hereditary disorder
- 2Hereditary spastic paraplegia
- 3Autosomal hereditary disorder
- 3Chronic myelopathy
- 3Chronic paraplegia
- 3Hereditary degenerative disease of central nervous system
- 3Spastic paraplegia
- 4Chronic nervous system disorder
- 4Degenerative disease of the central nervous system
- 4Hereditary disease
- 4Hereditary disorder of nervous system
- 4Paraplegia
- 4Spastic syndrome
- 4Spinal cord disease
- 5Bilateral lower limb paralytic syndrome
- 5Chronic disease
- 5Complete bilateral paralysis
- 5Degenerative disorder
- 5Disorder of nervous system
- 5Disorder of spinal region
- 5Disorder of the central nervous system
- 5Finding of spinal cord
- 5Genetic disease
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