acute episodes of neuropathic symptoms Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Neuropathic symptoms include numbness, dysesthesias, and a characteristic form of pain (neuralgia). (Human Phenotype Ontology, HP_0003489)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003489
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Genes

2 genes associated with the acute episodes of neuropathic symptoms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CPOX coproporphyrinogen oxidase
HMBS hydroxymethylbilane synthase