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#607677 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I; CMT2I
Cytogenetic locations: 10764043
Gene summaries Genetic tests Medical literature
*601097 - PERIPHERAL MYELIN PROTEIN 22; PMP22
Cytogenetic locations: -
*304040 - GAP JUNCTION PROTEIN, BETA-1; GJB1
Cytogenetic locations: Xp21.2
#162500 - NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP
*159440 - MYELIN PROTEIN ZERO; MPZ
Cytogenetic locations: 11709914
#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
#118200 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B
Cytogenetic locations: 15027400
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