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NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 DEJERINE-SOTTAS SYNDROME, SPORADIC DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT MYELIN GLYCOPROTEIN P-ZERO CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, WITH FOCALLY FOLDED MYELIN SHEATHS MPZ ROUSSY-LEVY SYNDROME CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B MPP MYELIN PROTEIN, PERIPHERAL CHARCOT-MARIE-TOOTH DISEASE, TYPE 2J CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D DEJERINE-SOTTAS SYNDROME, AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE, TYPE 2I P0
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