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WNT4

Wnt family member 4

gene with protein productOMIM: 6034903 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in2
SERKAL syndromeORPHA:139466
→
Müllerian aplasia and hyperandrogenismORPHA:247768
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Герминативная мутация (причина)1
Mayer-Rokitansky-Küster-Hauser syndrome type 2ORPHA:2578
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Данные: Orphadata (CC-BY-4.0)