Jump to:
loading...| Preferred Name |
Corneal dystrophy |
| ID |
http://www.orpha.net/ORDO/Orphanet_34533 |
| definition |
A heterogeneous group of bilateral, genetically determined, non-inflammatory eye diseases that are usually restricted to the cornea. The designation is imprecise but remains in use because of its clinical value. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=34533 |
| has_age_of_onset |
All ages |
| has_inheritance |
Mitochondrial inheritance X-linked recessive Autosomal recessive Not applicable Autosomal dominant |
| hasDbXref |
UMLS:C0010036 MedDRA:10011005 ICD-11:9A70 MeSH:D003317 ICD-10:H18.5 |
| label |
Corneal dystrophy |
| notation |
ORPHA:34533 Category |
| prefixIRI |
ORDO:Orphanet_34533 |
| prefLabel |
Corneal dystrophy |
| present_in |
Worldwide AND has_point_prevalence_range : Unknown United States AND has_point_prevalence_average_value : 110.0 AND has_point_prevalence_range : >1 / 1000 |
| subClassOf |
Create New Mapping