OMOP Concept 36714451
Multiple epiphyseal dysplasia Beighton type
StandardConditionSNOMED719689005Disorder
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 Multiple epiphyseal dysplasia Beighton type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 719689005 | Multiple epiphyseal dysplasia with myopia and deafness syndrome | Non-standard |
Synonyms
Alternative names recorded for Multiple epiphyseal dysplasia Beighton type across source vocabularies.
- displasia epifisaria múltiple tipo Beighton
- displasia epifisaria múltiple tipo Beighton (trastorno)
- Multiple epiphyseal dysplasia Beighton type (disorder)
- Multiple epiphyseal dysplasia with myopia and deafness syndrome
- síndrome de displasia epifisaria múltiple con miopía y sordera
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(66)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Autosomal dominant hereditary disorder
- 1Chronic deafness
- 1Congenital conductive hearing loss
- 1Multiple epiphyseal dysplasia
- 2Autosomal hereditary disorder
- 2Chronic disease of ear
- 2Conductive hearing loss
- 2Congenital anomaly of ear with impairment of hearing
- 2Decreased hearing
- 2Disorder of auditory system
- 2Epiphyseal dysplasia
- 2Hearing loss
- 2Hereditary disorder by system
- 2Spondyloepiphyseal dysplasia tarda
- 3Chronic disease
- 3Chronic disease of musculoskeletal system
- 3Congenital anomaly of skeletal bone
- 3Congenital hearing disorder
- 3Congenital malformation of ear
- 3Decline in functional status
- 3Developmental hereditary disorder
- 3Disorder of body system
- 3Disorder of ear
- 3Disorder of epiphysis
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