loading...| Preferred Name | Cogan syndrome | |
| Synonyms |
Cogan syndrome Cogan's syndrome diffuse interstitual keratitis |
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| Definitions |
Cogan syndrome (CS) is a rare autoimmune disorder of unknown origin characterized by inflammatory ocular disease (mainly interstitial keratitis) and vestibulo-auditory manifestations (mainly acute onset hearing loss, tinnitus and vertigo), in the setting of a negative work-up for syphilis, with a variable risk of developing into a systemic disease. Systemic manifestations may occur in more than 70% of cases. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0015453 |
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| closeMatch | ||
| database_cross_reference |
GARD:1421 DOID:0060216 SCTID:405810005 UMLS:C0271270 Orphanet:1467 MedDRA:10056667 MESH:D055952 |
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| definition |
Cogan syndrome (CS) is a rare autoimmune disorder of unknown origin characterized by inflammatory ocular disease (mainly interstitial keratitis) and vestibulo-auditory manifestations (mainly acute onset hearing loss, tinnitus and vertigo), in the setting of a negative work-up for syphilis, with a variable risk of developing into a systemic disease. Systemic manifestations may occur in more than 70% of cases. |
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| exactMatch |
http://identifiers.org/snomedct/405810005 http://identifiers.org/mesh/D055952 http://purl.obolibrary.org/obo/DOID_0060216 |
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| has characteristic | ||
| has_exact_synonym |
Cogan syndrome Cogan's syndrome diffuse interstitual keratitis |
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| id |
MONDO:0015453 |
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| in_subset |
http://purl.obolibrary.org/obo/mondo#ordo_disease http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#nord_rare |
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| label |
Cogan syndrome |
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| notation |
MONDO:0015453 |
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| prefLabel |
Cogan syndrome |
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| treeView | ||
| subClassOf |