OMOP Concept 44783873
Brown-Vialetto-Van Laere syndrome
StandardConditionSNOMED699866005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Brown-Vialetto-Van Laere syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537111 | Brown-Vialetto-Van Laere syndrome | Non-standard |
Synonyms
Alternative names recorded for Brown-Vialetto-Van Laere syndrome across source vocabularies.
- parálisis bulbar progresiva con sordera neurosensorial
- parálisis bulbar progresiva con sordera neurosensorial (trastorno)
- parálisis pontobulbar con sordera
- Pontobulbar palsy with deafness
- Progressive bulbar palsy with sensorineural deafness
- Progressive bulbar palsy with sensorineural deafness (disorder)
- Riboflavin transporter deficiency
- síndrome de Brown-Vialetto-van Laere
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Hereditary disorder of nervous system
- 1Hereditary hearing loss
- 1Progressive bulbar palsy
- 1Sensorineural hearing loss
- 2Auditory system hereditary disorder
- 2Autosomal hereditary disorder
- 2Disorder of brain stem
- 2Disorder of nervous system
- 2Hearing loss
- 2Hereditary disorder by system
- 2Multiple cranial nerve lesions and linked syndromes
- 2Upper motor neuron disease
- 3Cranial nerve disorder
- 3Disorder of auditory system
- 3Disorder of body system
- 3Disorder of brain
- 3Disorder of the central nervous system
- 3Hearing disorder
- 3Hereditary disease
- 3Motor neuron disease
- 4Central nervous system finding
- 4Disease
- 4Disorder of head
- 4Ear and auditory finding
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