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Cogan-Reese syndrome

Orpha number	ORPHA98980
Synonym(s)	-
Prevalence	-
Inheritance	-
Age of onset	-

ICD-10	H21.1
OMIM	-
UMLS	C1168173
MeSH	-
MedDRA	10059200
SNOMED CT	404633004

Summary

Cogan-Reese syndrome is a clinical variant of iridocorneal endothelial (ICE) syndrome (see this term) characterized by variable iris atrophy, pigmented and pedunculated nodules on the iris and corneal abonormalities. Secondary glaucoma is also a common complication of the disease.

Last update: February 2012

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