OMOP Concept 4213367
Thiel-Behnke corneal dystrophy
StandardConditionSNOMED417065002Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2005
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Thiel-Behnke corneal dystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535942 | Corneal dystrophy, Thiel-Behnke type | Non-standard |
| Nebraska Lexicon | 417065002 | CDB type II-Corneal dystrophy of Bowman's membrane, type II | Non-standard |
Synonyms
Alternative names recorded for Thiel-Behnke corneal dystrophy across source vocabularies.
- CDB type II-Corneal dystrophy of Bowman's membrane, type II
- distrofia corneal de la membrana de Bowman, tipo II
- distrofia corneal de Thiel-Behnke
- distrofia corneal de Thiel-Behnke (trastorno)
- Thiel-Behnke corneal dystrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Bowman's membrane finding
- 1Hereditary corneal dystrophy
- 2Autosomal hereditary disorder
- 2Corneal dystrophy
- 2Corneal finding
- 2Hereditary disorder of the visual system
- 3Anterior segment finding
- 3Corneal degeneration
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Visual system disorder
- 4Degenerative disorder of eye
- 4Disorder of body system
- 4Disorder of cornea
- 4Eye / vision finding
- 4Genetic disease
- 4Globe finding
- 5Anomaly of eye
- 5Clinical finding
- 5Degenerative disorder
- 5Disease
- 5Disorder of anterior segment of eye
- 5Finding of head region
- 6Disorder of eye
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