fibular aplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the fibula. (Human Phenotype Ontology, HP_0002990)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002990
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Genes

8 genes associated with the fibular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
BMPR1B bone morphogenetic protein receptor, type IB
FLNB filamin B, beta
GDF5 growth differentiation factor 5
LMBR1 limb development membrane protein 1
RBM8A RNA binding motif protein 8A
TBX15 T-box 15
WNT7A wingless-type MMTV integration site family, member 7A