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#145900 - HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS
Cytogenetic locations: 1p36, 1p36, 1p36
Gene summaries Genetic tests Medical literature
#607678 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D
Cytogenetic locations: 601332
*605725 - PERIAXIN; PRX
Cytogenetic locations: 22847150
#605253 - NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE; CHN1
NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL DOMINANT, INCLUDED
*601097 - PERIPHERAL MYELIN PROTEIN 22; PMP22
Cytogenetic locations: 612341
*304040 - GAP JUNCTION PROTEIN, BETA-1; GJB1
Cytogenetic locations: 11964417
#266500 - REFSUM DISEASE, CLASSIC
Cytogenetic locations: 10951529
#162500 - NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP
*159440 - MYELIN PROTEIN ZERO; MPZ
Cytogenetic locations: 11709914
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