abnormal number of permanent teeth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an altered number of of permanent teeth. (Human Phenotype Ontology, HP_0011044)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011044
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7 genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KCTD1 potassium channel tetramerization domain containing 1
MSX1 msh homeobox 1
OFD1 oral-facial-digital syndrome 1
RAB23 RAB23, member RAS oncogene family
RECQL4 RecQ protein-like 4
UBR1 ubiquitin protein ligase E3 component n-recognin 1
WNT10A wingless-type MMTV integration site family, member 10A