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GENATLAS PHENOTYPE

last update : 03-12-2020

Symbol	RP90
Location	15q25.1
Name	retinitis pigmentosa 90
Corresponding gene	IDHA3
Main clinical features	early-onset night blindness, within the first decade of life; also other typical features of RP, including retinal vessel attenuation, optic disc pallor, and retinal pigment epithelium (RPE) atrophy and pigmentation abnormalities
Genetic determination	autosomal recessive
Function/system disorder	eye
Type	disease

Remark(s)