Fibular hypoplasia and complex brachydactyly Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal recessive disease that is characterised by severe reduction or absence of the fibula and complex brachydactyly. (Human Disease Ontology, DOID_0050790)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537931
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Genes

1 genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GDF5 growth differentiation factor 5 2.88009