aplasia/hypoplasia of the tibia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the tibia. (Human Phenotype Ontology, HP_0005772)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005772
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12 genes associated with the aplasia/hypoplasia of the tibia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EIF4A3 eukaryotic translation initiation factor 4A3
GDF5 growth differentiation factor 5
GPC6 glypican 6
HYLS1 hydrolethalus syndrome 1
IHH indian hedgehog
LIFR leukemia inhibitory factor receptor alpha
LMBR1 limb development membrane protein 1
MIPOL1 mirror-image polydactyly 1
NEK1 NIMA-related kinase 1
SHOX short stature homeobox
TCTN3 tectonic family member 3
ZBTB16 zinc finger and BTB domain containing 16