OMOP Concept 4134123
Hereditary sensory and autonomic neuropathy
StandardConditionSNOMED128205005Disorder
Maps from
2
Descendants
25
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 Hereditary sensory and autonomic neuropathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138741 | Hereditary sensory and autonomic neuropathy | Non-standard |
| MeSH | D009477 | Hereditary Sensory and Autonomic Neuropathies | Non-standard |
Synonyms
Alternative names recorded for Hereditary sensory and autonomic neuropathy across source vocabularies.
- Hereditary sensory and autonomic neuropathy (disorder)
- HSAN - hereditary sensory and autonomic neuropathy
- neuropatía sensitiva y autónoma hereditaria
- neuropatía sensitiva y autónoma hereditaria (trastorno)
- NSAH - neuropatía sensitiva y autonómica hereditaria
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Hereditary peripheral neuropathy
- 1Inherited autonomic nervous system disorder
- 1Neuropathy
- 2Disorder of autonomic nervous system
- 2Disorder of nervous system
- 2Disorder of the peripheral nervous system
- 2Hereditary disorder of nervous system
- 3Disorder of body system
- 3Hereditary disorder by system
- 4Disease
- 4Hereditary disease
- 5Clinical finding
- 5Genetic disease
Narrower concepts
(25)Included automatically when you query with descendants.
- 1Autosomal dominant sensory neuropathy
- 1Congenital insensitivity to pain, anosmia, neuropathic arthropathy
- 1Congenital insensitivity to pain, hyperhidrosis, absence of cutaneous sensory innervation
- 1Congenital insensitivity to pain with severe intellectual disability
- 1Congenital sensory neuropathy with selective loss of small myelinated fibers
- 1Familial dysautonomia
- 1Hereditary dysautonomia with motor neuropathy
- 1Hereditary insensitivity to pain with anhidrosis
- 1Hereditary sensory and autonomic neuropathy due to TECPR2 mutation
- 1Hereditary sensory and autonomic neuropathy type 6
- 1Hereditary sensory and autonomic neuropathy type 7
- 1Hereditary sensory and autonomic neuropathy type 8
- 1Hereditary sensory and autonomic neuropathy type I
- 1Hereditary sensory and autonomic neuropathy type II
- 1Hereditary sensory and autonomic neuropathy with deafness and global delay
- 1Hereditary sensory and autonomic neuropathy with spastic paraplegia
- 1X-linked hereditary sensory and autonomic neuropathy with deafness
- 2Hereditary sensory and autonomic neuropathy type 1B
- 2Hereditary sensory autonomic neuropathy type IA
- 2Hereditary sensory autonomic neuropathy type IC
- 2Hereditary sensory autonomic neuropathy type ID
- 2Hereditary sensory autonomic neuropathy type IE
- 2Hereditary sensory autonomic neuropathy type IIA
- 2Hereditary sensory autonomic neuropathy type IIB
- 2Hereditary sensory autonomic neuropathy type IIC
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