OMOP Concept 4301399
Albinism-deafness syndrome of Tietz
StandardConditionSNOMED403805009Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Albinism-deafness syndrome of Tietz via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536919 | Tietz syndrome | Non-standard |
Synonyms
Alternative names recorded for Albinism-deafness syndrome of Tietz across source vocabularies.
- Albinism-deafness syndrome of Tietz (disorder)
- síndrome de albinismo y sordera de Tietz
- síndrome de albinismo y sordera de Tietz (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(43)Roll up to these when you need a wider cohort.
- 1Albinism
- 1Autosomal dominant hereditary disorder
- 1Congenital sensorineural hearing loss
- 1Hereditary hearing loss
- 1Profound sensorineural hearing loss
- 1Sensorineural hearing loss of bilateral ears
- 2Auditory system hereditary disorder
- 2Autosomal hereditary disorder
- 2Bilateral disorder of ears
- 2Congenital hearing disorder
- 2Congenital malformation
- 2Developmental hereditary disorder
- 2Disorder of pigmentation
- 2Hearing loss
- 2Inborn error of metabolism
- 2Profound hearing loss
- 2Sensorineural hearing loss
- 3Congenital disease
- 3Developmental disorder
- 3Disease
- 3Disorder of auditory system
- 3Disorder of left ear
- 3Disorder of right ear
- 3Hearing disorder
- 3Hereditary disease
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