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Browse result for Dejerine-Sottas syndrome

※ introduction

    Dejerine¨CSottas disease, also known as, Dejerine¨CSottas syndrome,[3] hereditary motor and sensory polyneuropathy type III, and Charcot¨CMarie¨CTooth disease type 3, is a hereditary neurological disorder characterized by damage to the peripheral nerves, demyelination, and resulting progressive muscle wasting and somatosensory loss. The condition is caused by mutations in various genes and currently has no known cure.[2]

Reference
Wiki: Dejerine-Sottas syndrome



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD04623P251894359
MPZ
Myelin protein P0
Homo sapiens
PTMD06108Q014535376
PMP22
Peripheral myelin protein 22
Homo sapiens