OMOP Concept 4319472
Peripheral motor neuropathy
StandardConditionSNOMED95663000Disorder
Maps from
2
Descendants
21
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Peripheral motor neuropathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 114224 | Motor neuritis | Non-standard |
| Nebraska Lexicon | 95663000 | Peripheral motor neuropathy | Non-standard |
Synonyms
Alternative names recorded for Peripheral motor neuropathy across source vocabularies.
- Motor neuritis
- Motor peripheral neuropathy
- neuritis motora
- neuropatía motora periférica
- neuropatía motora periférica (trastorno)
- Peripheral motor neuropathy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(6)Roll up to these when you need a wider cohort.
Narrower concepts
(21)Included automatically when you query with descendants.
- 1Asymmetric proximal motor neuropathy due to diabetes mellitus
- 1Autoimmune peripheral motor neuropathy
- 1Autosomal dominant distal hereditary motor neuropathy
- 1Autosomal recessive distal hereditary motor neuropathy
- 1Symmetric proximal motor neuropathy due to diabetes mellitus
- 1X-linked distal hereditary motor neuropathy
- 2Autosomal dominant congenital benign spinal muscular atrophy
- 2Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome
- 2Autosomal dominant spastic paraplegia type 17
- 2Autosomal recessive distal spinal muscular atrophy type 3
- 2Distal hereditary motor neuropathy Jerash type
- 2Distal hereditary motor neuropathy type 1
- 2Distal hereditary motor neuropathy type 2
- 2Distal hereditary motor neuropathy type 5
- 2Distal hereditary motor neuropathy type 7
- 2Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome
- 2Spinal muscular atrophy with respiratory distress type 1
- 2Spinal muscular atrophy with respiratory distress type 2
- 2X-linked distal arthrogryposis multiplex congenita
- 2X-linked distal spinal muscular atrophy type 3
- 2Young adult-onset distal hereditary motor neuropathy
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