acute demyelinating polyneuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Acute progressive areflexic weakness and mild sensory changes resulting from myelin breakdown and axonal degeneration. (Human Phenotype Ontology, HP_0007131)
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1 genes associated with the acute demyelinating polyneuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PMP22 peripheral myelin protein 22