Summary
Meacham Syndrome, also known as rhabdomyomatous dysplasia-cardiopathy-genital anomalies syndrome,is related to meacham winn culler syndrome and congenital diaphragmatic hernia,and has symptoms including ambiguous genitalia, abnormality of the vagina and congenital diaphragmatic hernia. An important gene associated with Meacham Syndrome is WT1 (Wilms Tumor 1). Affiliated tissues include heart, uterus and lung
All SNPs
Genes | SNP | Risk Alleles |
---|