OMOP Concept 605187
Retinitis pigmentosa-deafness syndrome type 3
StandardConditionSNOMED1010610007Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2021
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Retinitis pigmentosa-deafness syndrome type 3 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | Q99.813 | Usher syndrome, type 3 | Non-standard |
Synonyms
Alternative names recorded for Retinitis pigmentosa-deafness syndrome type 3 across source vocabularies.
- Retinitis pigmentosa-deafness syndrome type 3 (disorder)
- síndrome de retinitis pigmentaria - sordera tipo 3
- síndrome de retinitis pigmentaria - sordera tipo 3 (trastorno)
- síndrome de Usher tipo 3
- Usher syndrome type 3
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(46)Roll up to these when you need a wider cohort.
- 1Retinitis pigmentosa-deafness syndrome
- 2Auditory system hereditary disorder
- 2Autosomal recessive retinitis pigmentosa
- 2Congenital malformation
- 2Congenital sensorineural hearing loss
- 2Developmental hereditary disorder
- 3Autosomal recessive hereditary disorder
- 3Congenital disease
- 3Congenital hearing disorder
- 3Developmental disorder
- 3Disorder of auditory system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Retinitis pigmentosa
- 3Sensorineural hearing loss
- 4Autosomal hereditary disorder
- 4Disease
- 4Disorder of body system
- 4Disorder of fetus and/or newborn
- 4Ear and auditory finding
- 4Genetic disease
- 4Hearing disorder
- 4Hearing loss
- 4Hereditary retinal dystrophy
- 5Clinical finding
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