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
Disease Interacts with Genes
Disease Interacts with Substances
Processes Associated With Trait
Molecular Function Associated With Trait
Biological Processes Associated With Trait
Pathways Associated With Trait
Symptoms Associated With Trait
Selected genes are highlighted in orange, bookmarked
genes are green
- Chemical increases gene,
- Chemical decreases gene,
- Chemical increases and decreases gene simultaneosly,
No arrows - gene doesn't interact with the chemical.
- Gene should be increased/decreased most of the time and the chemical does it.
- Gene should be increased/decreased most of the time but the chemical does the opposite.