upper limb muscle weakness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Weakness of the muscles of the arms. (Human Phenotype Ontology, HP_0003484)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003484
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9 genes associated with the upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
EGR2 early growth response 2
FGD4 FYVE, RhoGEF and PH domain containing 4
GARS glycyl-tRNA synthetase
LMNA lamin A/C
MPZ myelin protein zero
SH3TC2 SH3 domain and tetratricopeptide repeats 2
TCAP titin-cap
YARS tyrosyl-tRNA synthetase