RS104894342 FGF23
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What This Variant Does
"[OMIM:?]
Associated Conditions
Tumoral calcinosis
hyperphosphatemic
familial
1
2
Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
Autosomal dominant hypophosphatemic rickets
Tumoral calcinosis
hyperphosphatemic
familial
1
2
Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
Autosomal dominant hypophosphatemic rickets
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