|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Acute progressive areflexic weakness and mild sensory changes resulting from myelin breakdown and axonal degeneration. (Human Phenotype Ontology, HP_0007131)|
|Downloads & Tools|
1 genes associated with the acute demyelinating polyneuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|PMP22||peripheral myelin protein 22|