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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Corneal Dystrophies, Hereditary [Disease/Finding] | |
| Synonyms |
Corneal Dystrophies, Hereditary |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000000852 |
|
| altLabel |
Corneal Dystrophies, Hereditary
|
|
| cui |
C0010035
|
|
| MESH DEFINITION |
Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect.
|
|
| MESH DUI |
D003317
|
|
| MeSH name |
Corneal Dystrophies, Hereditary
|
|
| MESH UI |
M0005178
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|
| NDFRT kind |
DISEASE_KIND
|
|
| notation |
N0000000852
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|
| NUI |
N0000000852
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|
| prefLabel |
Corneal Dystrophies, Hereditary [Disease/Finding]
|
|
| SNOMED CID |
77797009 193832003
|
|
| tui |
T047
|
|
| subClassOf |
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