ectopic ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Formation of abnormal, extraskeletal bony tissue, i.e., the presence of bone in soft tissue where bone normally does not exist. (Human Phenotype Ontology, HP_0011986)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011986
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Genes

2 genes associated with the ectopic ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
NT5E 5'-nucleotidase, ecto (CD73)