loading...| Preferred Name |
Iridocorneal endothelial syndrome |
|
| Synonyms |
ICE syndrome |
|
| Definitions |
Iridocorneal endothelial (ICE) syndrome describes a group of progressive corneal proliferative endotheliopathies comprised of Chandlers syndrome, Cogan-Reese syndrome and essential iris atrophy (see these terms), affecting mainly young adult females and characterized by iris holes and atrophy, papillary distortion, anterior synechiae, corneal edema and often with secondary glaucoma and corneal decompensation as complications |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_64734 |
|
| alternative_term |
ICE syndrome |
|
| definition |
Iridocorneal endothelial (ICE) syndrome describes a group of progressive corneal proliferative endotheliopathies comprised of Chandlers syndrome, Cogan-Reese syndrome and essential iris atrophy (see these terms), affecting mainly young adult females and characterized by iris holes and atrophy, papillary distortion, anterior synechiae, corneal edema and often with secondary glaucoma and corneal decompensation as complications |
|
| definition_citation |
Orphanet |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=64734 |
|
| has_age_of_onset |
Adult |
|
| has_inheritance |
Not applicable |
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| hasDbXref |
MeSH:D057129 MedDRA:10053678 ICD-11:LA11.Y UMLS:C1096100 ICD-10:H21.1 |
|
| label |
Iridocorneal endothelial syndrome |
|
| notation |
ORPHA:64734 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_64734 |
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| prefLabel |
Iridocorneal endothelial syndrome |
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| present_in |
Worldwide AND has_point_prevalence_range : Unknown |
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| treeView | ||
| subClassOf |