Orphanet: Cogan Reese syndrome

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Cogan-Reese syndrome

Disease definition

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.

ORPHA:98980

Synonym(s): -
Prevalence: -
Inheritance: -
Age of onset: -
ICD-10: H21.2
OMIM: -
UMLS: C1168173
MeSH: -
GARD: 6125
MedDRA: 10059200

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Cogan-Reese syndrome

ORPHA:98980

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