Meacham Syndrome, also known as rhabdomyomatous dysplasia-cardiopathy-genital anomalies syndrome, is related to septate vagina and frasier syndrome. An important gene associated with Meacham Syndrome is WT1 (WT1 Transcription Factor). Affiliated tissues include heart and uterus, and related phenotypes are congenital diaphragmatic hernia and aplasia/hypoplasia of the lungs