proximal lower limb amyotrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Muscular atrophy affecting proximally located muscles of the legs, i.e., of the thigh. (Human Phenotype Ontology, HP_0008956)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008956
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Genes

4 genes associated with the proximal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANO5 anoctamin 5
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
HNRNPDL heterogeneous nuclear ribonucleoprotein D-like
TRPV4 transient receptor potential cation channel, subfamily V, member 4