Additional Disease Briefs

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myopia 6

Also known as: MYP6, SCO2 myopia (disease), myopia (disease) caused by mutation in SCO2, myopia 6, myopia type 6, myopia, susceptibility to




myosclerosis

Also known as: congenital myosclerosis, LC6wenthal type, congenital myosclerosis, Löwenthal type, myopathy, myosclerotic, myosclerosis, autosomal recessive, myosclerosis, congenital, myosclerosis, congenital, of Lowenthal


myospherulosis

Also known as: spherulocytosis, subcutaneous spherulocystic disease


myotonia fluctuans

Also known as: Fluctuating myotonia, MF, exercise-induced delayed-onset myotonia



myotonic dystrophy type 2

Also known as: CNBP myotonic dystrophy, DM2, PROMM, dystrophia myotonica 2, dystrophia myotonica type 2, myotonic dystrophy 2, myotonic dystrophy caused by mutation in CNBP, myotonic dystrophy type 2, myotonic myopathy, proximal, proximal myotonic dystrophy, proximal myotonic myopathy, ricker disease, ricker syndrome