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FGF23
fibroblast growth factor 23
gene with protein product
OMIM: 605380
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome
ORPHA:306661
→
Disease-causing germline mutation(s) (gain of function) in
1
Autosomal dominant hypophosphatemic rickets
ORPHA:89937
→
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Редкие заболевания
FGF23
🧬
FGF23
fibroblast growth factor 23
gene with protein product
OMIM: 605380
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome
ORPHA:306661
→
Disease-causing germline mutation(s) (gain of function) in
1
Autosomal dominant hypophosphatemic rickets
ORPHA:89937
→