Chain1560: Tumoral Calcinosis, Hyperphasphatemic, Familial
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 |
---|---|
FGF23 | chr12:4481788 |
GALNT3 | chr2:166626727,chr2:166611441,chr2:166611437 |