limited wrist movement Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal limitation of the mobility of the wrist. (Human Phenotype Ontology, HP_0006248)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006248
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Genes

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

Symbol Name
PIEZO2 piezo-type mechanosensitive ion channel component 2
SALL4 spalt-like transcription factor 4
SHOX short stature homeobox