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WNT7A

Wnt family member 7A

gene with protein productOMIM: 6015702 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in2
Phocomelia, Schinzel typeORPHA:2879
→
Fuhrmann syndromeORPHA:2854
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Данные: Orphadata (CC-BY-4.0)