Chain796: Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome
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 |
---|---|
SLC25A15 | chr13:41381512,chr13:41373349,chr13:41381539 |