Chain1173: Night Blindness, Congenital Stationary, Type 2

This is a rare disease.

Example use A

Rare disease screening of newborns or adults thinking of having children. Could also be used as part of a comprehensive analysis of a person's genes.

Developer

Dr. Colby

Genetic info

GenesGenetic variants
CACNA1FchrX:49084510,chrX:49074970,chrX:49072945

Qualitative

Type

text

Possible responses

Carrier, Possibly Affected, Not Detected, insufficient data, error