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GENATLAS PHENOTYPE

last update : 11-07-2023

Symbol	OCA8
Location	13q32.1
Name	oculocutaneous albinism, type VIII
Corresponding gene	DCT
Main clinical features	mild hair and skin hypopigmentation, associated with ocular features including nystagmus, reduced visual acuity, iris transillumination, and hypopigmentation of the retina
Genetic determination	autosomal recessive
Function/system disorder	dermatology
	eye
Type	disease

Remark(s)