progressive distal muscular atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Progressive muscular atrophy affecting muscles in the distal portions of the extremities. (Human Phenotype Ontology, HP_0008955)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008955
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Genes

2 genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASAH1 N-acylsphingosine amidohydrolase (acid ceramidase) 1
TRPV4 transient receptor potential cation channel, subfamily V, member 4