aplasia/hypoplasia of the tarsal bones Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the tarsal bones. (Human Phenotype Ontology, HP_0008363)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008363
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3 genes associated with the aplasia/hypoplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HDAC6 histone deacetylase 6
LMBR1 limb development membrane protein 1
WNT7A wingless-type MMTV integration site family, member 7A