Chain1322: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, 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
SLC25A4chr4:186066117,chr4:186066146

Qualitative

Type

text

Possible responses

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