Summary

Fuhrmann Syndrome, also known as fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly,is related to fibular aplasia and fibular aplasia ectrodactyly,and has symptoms including talipes, femoral bowing and hypoplasia of the radius. An important gene associated with Fuhrmann Syndrome is WNT7A (Wnt Family Member 7A). Affiliated tissues include bone, liver and uterus

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Pathways Associated With Trait

Symptoms Associated With Trait