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VMD2 (medical condition): A rare inherited eye disorder that affects the retina and often results in progressive loss of central vision. Peripheral vision and night-vision are spared.
See also:
Macular dystrophy, vitelliform:
»Introduction: Macular dystrophy, vitelliform
»Symptoms of Macular dystrophy, vitelliform
VMD2 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that VMD2, or a subtype of VMD2,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
VMD2: Another name for Macular dystrophy, vitelliform (or close medical condition association).
»Introduction: Macular dystrophy, vitelliform
»Symptoms of Macular dystrophy, vitelliform
Some of the symptoms of VMD2 incude:
Read more about symptoms of VMD2 (Macular dystrophy, vitelliform)
These medical disease topics may be related to VMD2:
Source - NIH
Search to find out more about VMD2:
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