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*601097 - PERIPHERAL MYELIN PROTEIN 22; PMP22
Cytogenetic locations: 131370
Gene summaries Genetic tests Medical literature
#180800 - ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA
Cytogenetic locations: 1p36, 1p36
#162500 - NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP
#145900 - HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS
Cytogenetic locations: 1p36, 1p36, 1p36
#139393 - GUILLAIN-BARRE SYNDROME, FAMILIAL; GBS
POLYNEUROPATHY, INFLAMMATORY DEMYELINATING, CHRONIC, INCLUDED; CIDP, INCLUDED
#118300 - CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS
#118220 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A
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