CDGG1 (medical condition): A rare genetic condition affecting the corneas can resulting in impaired vision usually by fifth or sixth decade.
See also:
Groenouw type I corneal dystrophy:
»Introduction: Groenouw type I corneal dystrophy
»Symptoms of Groenouw type I corneal dystrophy
CDGG1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that CDGG1, or a subtype of CDGG1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
CDGG1: Another name for Groenouw type I corneal dystrophy (or close medical condition association).
»Introduction: Groenouw type I corneal dystrophy
»Symptoms of Groenouw type I corneal dystrophy
Some of the symptoms of CDGG1 incude:
Read more about symptoms of CDGG1 (Groenouw type I corneal dystrophy)
Source - NIH
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