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GENATLAS PHENOTYPE

last update : 26-10-2018

Symbol	ARCC7
Location	9q22.33
Name	congenital cataract, autosomal recessive 7
Other name(s)	cataract multiple type 36
Corresponding gene	TDRD7
Other symbol(s)	CTRCT36
Main clinical features	autosomal recessive congenital cataract cataracts present at birth or developed in infancy bilateral membranous cataracts accompanied by other ocular abnormalities, including corneal opacity, microcornea, and nystagmus
Genetic determination	autosomal recessive
Function/system disorder	eye
Type	disease

Remark(s)