WNT4 (Wnt Family Member 4) is a Protein Coding gene. Diseases associated with WNT4 include Serkal Syndrome and Mullerian Aplasia And Hyperandrogenism. Among its related pathways are Transcription Androgen Receptor nuclear signaling and BMP2-WNT4-FOXO1 Pathway in Human Primary Endometrial Stromal Cell Differentiation.