OMOP Concept 4319117
Congenital anomaly of the peripheral nervous system
StandardConditionSNOMED22133005Disorder
Maps from
2
Descendants
39
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 Congenital anomaly of the peripheral nervous system via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144174 | Congenital Anomaly of the Peripheral Nervous System | Non-standard |
| Nebraska Lexicon | 22133005 | Congenital anomaly of the peripheral nervous system | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of the peripheral nervous system across source vocabularies.
- anomalía congénita del sistema nervioso periférico
- anomalía congénita del sistema nervioso periférico (trastorno)
- Congenital anomaly of the peripheral nervous system (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(39)Included automatically when you query with descendants.
- 1Congenital aganglionic megacolon
- 1Congenital anomaly of peripheral nerve
- 1Congenital cataracts, facial dysmorphism and neuropathy
- 2Aganglionosis of Auerbach's plexus
- 2Congenital anomaly of cauda equina
- 2Congenital deficiency of cochlear nerve
- 2Congenital hypoganglionosis of large intestine
- 2Congenital polyneuropathy
- 2Developmental displacement of brachial plexus
- 2Duane's syndrome
- 2Extensive aganglionosis Hirschsprung disease
- 2Goldberg Shprintzen megacolon syndrome
- 2Haddad syndrome
- 2Hirschsprung disease of rectosigmoid region
- 2Hirschsprung disease with deafness and polydactyly syndrome
- 2Hirschsprung disease with nail hypoplasia and dysmorphism
- 2Hirschsprung disease with type D brachydactyly syndrome
- 2Immature ganglionosis of large intestine
- 2Isolated hereditary congenital facial paralysis
- 2Long segment Hirschsprung's disease
- 2Mowat-Wilson syndrome
- 2Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
- 2Short segment Hirschsprung's disease
- 2Total intestinal aganglionosis
- 2Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome
- 2Waardenburg Shah syndrome
- 3Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy
- 3Duane-radial ray syndrome
- 3Duane's syndrome of left eye
- 3Duane's syndrome of right eye
- 3Duane's syndrome, type 1
- 3Duane's syndrome, type 2
- 3Duane's syndrome, type 3
- 3Duane syndrome with vertical deviation
- 3Mowat-Wilson syndrome due to monosomy 2q22
- 3Wildervanck syndrome
- 4Bilateral Duane's syndrome of eyes
- 4Duane anomaly, myopathy, scoliosis syndrome
- 4Duane retraction syndrome with congenital deafness
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