OMOP Concept 36716461
Thickened earlobe with conductive deafness syndrome
StandardConditionSNOMED722476007Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Thickened earlobe with conductive deafness syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 722476007 | Thickened earlobe with conductive deafness syndrome | Non-standard |
Synonyms
Alternative names recorded for Thickened earlobe with conductive deafness syndrome across source vocabularies.
- Escher Hirt syndrome
- síndrome de engrosamiento de lóbulo auricular con sordera de conducción
- síndrome de engrosamiento de lóbulo auricular con sordera de conducción (trastorno)
- síndrome de Escher Hirt
- Thickened earlobe with conductive deafness syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(65)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Autosomal dominant hereditary disorder
- 1Conductive hearing loss
- 1Congenital anomaly of ear with impairment of hearing
- 1Congenital micrognathism
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Microtia
- 1Multiple malformation syndrome with facial defects as major feature
- 2Autosomal hereditary disorder
- 2Congenital abnormality of external ear
- 2Congenital anomaly of face
- 2Congenital anomaly of mandible
- 2Congenital hearing disorder
- 2Congenital malformation of ear
- 2Craniofacial microsomia
- 2Developmental disorder
- 2Disorder of auditory system
- 2Disorder of ear
- 2Disorder of musculoskeletal system
- 2Hearing loss
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hypoplasia of mandibular bone
- 2Multiple system malformation syndrome
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