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

GenesGenetic variants
FGF23chr12:4481788
GALNT3chr2:166626727,chr2:166611441,chr2:166611437

Qualitative

Type

text

Possible responses

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