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
Genes | Genetic variants |
---|---|
SLC25A4 | chr4:186066117,chr4:186066146 |