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WNT7A
Wnt family member 7A
gene with protein product
OMIM: 601570
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Phocomelia, Schinzel type
ORPHA:2879
→
Fuhrmann syndrome
ORPHA:2854
→
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Редкие заболевания
WNT7A
🧬
WNT7A
Wnt family member 7A
gene with protein product
OMIM: 601570
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Phocomelia, Schinzel type
ORPHA:2879
→
Fuhrmann syndrome
ORPHA:2854
→