pseudoarthrosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A pathologic entity characterized by a developmental defect in a long bone leading to bending and pathologic fracture, with inability to form a normal bony callus with subsequent fibrous nonunion, leading to the pseudarthrosis (or false joint). (Human Phenotype Ontology, HP_0005864)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005864
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Genes

6 genes associated with the pseudoarthrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EFNB1 ephrin-B1
FGFR1 fibroblast growth factor receptor 1
LMNA lamin A/C
NF1 neurofibromin 1
WNT7A wingless-type MMTV integration site family, member 7A
ZMPSTE24 zinc metallopeptidase STE24