craniofacial osteosclerosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormally increased density of craniofacial bone tissue. (Human Phenotype Ontology, HP_0005464)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005464
Similar Terms
Downloads & Tools

Genes

3 genes associated with the craniofacial osteosclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
SOST sclerostin
TBCE tubulin folding cofactor E