aplasia/hypoplasia of the premaxilla Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the premaxilla. (Human Phenotype Ontology, HP_0010756)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010756
Similar Terms
Downloads & Tools


2 genes associated with the aplasia/hypoplasia of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GLI2 GLI family zinc finger 2
PTCH1 patched 1