ulnar deviation of the hand Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Divergence of the longitudinal axis of the hand at the wrist in a posterior (ulnar) direction (i.e., towards the little finger). (Human Phenotype Ontology, HP_0009487)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009487
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Genes

2 genes associated with the ulnar deviation of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COMP cartilage oligomeric matrix protein
LBR lamin B receptor