Chain1321: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions

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
PEO1chr10:102749073
POLGchr15:89873415,chr15:89873415,chr15:89872286,chr15:89870432,chr15:89868870,chr15:89868870

Qualitative

Type

text

Possible responses

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