OMOP Concept 4170096
Macular corneal dystrophy Type I
StandardConditionSNOMED418054005Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2006
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Macular corneal dystrophy Type I via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537834 | Macular dystrophy, corneal type 1 | Non-standard |
| Nebraska Lexicon | 418054005 | Macular corneal dystrophy Type I | Non-standard |
Synonyms
Alternative names recorded for Macular corneal dystrophy Type I across source vocabularies.
- distrofia corneal macular tipo I
- distrofia corneal macular tipo I (trastorno)
- Macular corneal dystrophy Type I (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Macular corneal dystrophy
- 2Autosomal recessive hereditary disorder
- 2Connective tissue hereditary disorder
- 2Developmental hereditary disorder
- 2Hereditary corneal dystrophy
- 2Stromal corneal dystrophy
- 3Autosomal hereditary disorder
- 3Corneal dystrophy
- 3Corneal stromal degeneration
- 3Developmental disorder
- 3Disorder of connective tissue
- 3Hereditary disease
- 3Hereditary disorder of the visual system
- 4Corneal degeneration
- 4Corneal stroma finding
- 4Disease
- 4Disorder of soft tissue
- 4Genetic disease
- 4Hereditary disorder by system
- 4Visual system disorder
- 5Clinical finding
- 5Corneal finding
- 5Degenerative disorder of eye
- 5Disorder of body system
- 5Disorder of cornea
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