congenital pseudoarthrosis of the clavicle Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The two portions of the clavicle (corresponding to the two primary ossification centers of the clavicle) are connected by a fibrous bridge that is contiguous with the periosteum, and a synovial membrane develops, resulting in a clavicle with a bipartite appearance radiographically. Congenital pseudarthrosis of the clavicle generally presents as a painless mass or swelling over the clavicle. (Human Phenotype Ontology, HP_0006585)
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4 genes associated with the congenital pseudoarthrosis of the clavicle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EFNB1 ephrin-B1
LMNA lamin A/C
WNT7A wingless-type MMTV integration site family, member 7A
ZMPSTE24 zinc metallopeptidase STE24