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FGF23

fibroblast growth factor 23

HCNC Approved Symbol
FGF23 (HGNC:3680)
Genomic Coordinates
12:4,368,227 - 4,379,712 (12p13.32)
Synonyms
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Hypophosphatemic rickets, autosomal dominant
193100AD
Tumoral calcinosis, hyperphosphatemic, familial, 2
617993AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the FGF23 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results