OMOP Concept 36713569
Branchiogenic deafness syndrome
StandardConditionSNOMED717944002Disorder
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 Branchiogenic deafness syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563780 | Branchiogenic-Deafness Syndrome | Non-standard |
| Nebraska Lexicon | 717944002 | Branchiogenic deafness syndrome | Non-standard |
Synonyms
Alternative names recorded for Branchiogenic deafness syndrome across source vocabularies.
- Branchiogenic deafness syndrome (disorder)
- Megarbane Loiselet syndrome
- síndrome branquigénico con sordera
- síndrome branquigénico con sordera (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Autosomal dominant hereditary disorder
- 1Congenital anomaly of ear with impairment of hearing
- 1Developmental hereditary disorder
- 1Multiple system malformation syndrome
- 2Autosomal hereditary disorder
- 2Congenital hearing disorder
- 2Congenital malformation of ear
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Disorder of auditory system
- 2Hearing loss
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Congenital anomaly of head
- 3Congenital disease
- 3Congenital malformation
- 3Disease
- 3Disorder of body system
- 3Disorder of ear
- 3Ear and auditory finding
- 3Genetic disease
- 3Hearing disorder
- 4Clinical finding
- 4Disorder of fetus and/or newborn
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