Chain1264: Peroxisome Biogenesis Disorder, Complementation Group 3
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 |
---|---|
PEX12 | chr17:33902922,chr17:33904914 |