Chain1217: Optic Atrophy, Deafness, Opthalmoplegia, and Myopathy

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
OPA1chr3:193361785
SPINK5rs2303067,chr5:147480027
IL4Rrs1801275

Qualitative

Type

text

Possible responses

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