loading...| Preferred Name | Cogan syndrome | |
| Synonyms |
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|
| Definitions |
A rare inflammatory/autoimmune disorder of unknown origin characterized by interstitial keratitis (IK) and audiovestibular dysfunctions. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_1467 |
|
| definition |
A rare inflammatory/autoimmune disorder of unknown origin characterized by interstitial keratitis (IK) and audiovestibular dysfunctions. |
|
| definition_citation |
Orphanet |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=1467 |
|
| has_age_of_onset |
Adolescent Adult Childhood |
|
| has_inheritance |
Not applicable |
|
| hasDbXref |
MedDRA:10056667 ICD-10:H16.3 ICD-11:4A44.Y UMLS:C0271270 MeSH:D055952 |
|
| label |
Cogan syndrome |
|
| notation |
ORPHA:1467 |
|
| part_of |
http://www.orpha.net/ORDO/Orphanet_519290 http://www.orpha.net/ORDO/Orphanet_156140 |
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| prefixIRI |
ORDO:Orphanet_1467 |
|
| prefLabel |
Cogan syndrome |
|
| present_in |
Worldwide AND has_cases/families_value : 300.0 (Case) Worldwide AND has_point_prevalence_range : Unknown |
|
| treeView |
http://www.orpha.net/ORDO/Orphanet_519290 http://www.orpha.net/ORDO/Orphanet_156140 |
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| subClassOf |