|
CHARCOT-MARIE-TOOTH DISEASE 1B (CMT1B)
|
CHARCOT-MARIE-TOOTH DISEASE 2I (CMT2I)
|
CHARCOT-MARIE-TOOTH DISEASE 2J (CMT2J)
|
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D
|
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT, INTERMEDIATE TYPE, D (CMTDID)
|
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B
|
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, INCLUDED
|
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, WITH FOCALLY FOLDED MYELIN SHEATHS
|
CHARCOT-MARIE-TOOTH DISEASE, TYPE 2I
|
CHARCOT-MARIE-TOOTH DISEASE, TYPE 2J
|
DEJERINE-SOTTAS SYNDROME (DSS)
|
DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
|
NEUROPATHY, CONGENITAL HYPOMYELINATING OR AMYELINATING (CHN)
|
NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL DOMINANT
|
ROUSSY-LEVY SYNDROME
|
ROUSSY-LEVY SYNDROME (ROULS)
|