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GENATLAS PHENOTYPE

last update : 20-03-2009

Symbol	OED
Location	Xp21.1
Name	blindness, night, congenital, stationary 2,
Other name(s)	Oregon eye disease Duchenne muscular dystrophy
Corresponding gene	DMD
Other symbol(s)	CSNBX3
Main clinical features	some incomplete forms, with persistence of slight rod function (dystrophin defect)
Genetic determination	sex linked
Function/system disorder
Type	disease

Gene product

Name	dystrophin (DMD)

Remark(s)