emg: axonal abnormality Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Electromyographic (EMG) findings characteristic of axonal neuropathy, with normal or slightly decreased nerve conduction velocities, normal or slightly prolonged distal latencies, but significantly reduced motor potentials and sensory amplitudes. There may be spontaneous activity upon needle EMG studies, such as increased insertional activity, positive sharp waves, and fibrillation potentials. (Human Phenotype Ontology, HP_0003482)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003482
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Genes

1 genes associated with the emg: axonal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1