widely-spaced maxillary central incisors Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased distance between the maxillary central permanent incisor tooth. (Human Phenotype Ontology, HP_0001566)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001566
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Genes

3 genes associated with the widely-spaced maxillary central incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALX3 ALX homeobox 3
ANKRD11 ankyrin repeat domain 11
ATRX alpha thalassemia/mental retardation syndrome X-linked