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GENATLAS PHENOTYPE

last update : 21/12/2007

Symbol	SCCD
Location	1p36.2
HGNC id	14431
Name	Schnyder cristalline corneal dystrophy
Other name(s)	corneal dystrophy, epithelial basement membrane . Cogan corneal dystrophy . corneal dystrophy, map-dot-fingerprint type
Corresponding gene	UBIAD1
Main clinical features	bilateral corneal clouding, arcus lipoides and anterior crystalline cholesterol deposition
Genetic determination	autosomal dominant
Function/system disorder	eye
Type	disease