Search on: HMSN 
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Descriptor English:   Hereditary Sensory and Motor Neuropathy 
Descriptor Spanish:   Neuropatía Hereditaria Motora y Sensorial 
Descriptor Portuguese:   Neuropatia Hereditária Motora e Sensorial 
Synonyms English:   CMT4f
Charcot Marie Tooth Disease, Type 3
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
Charcot-Marie-Tooth Disease, Type 3
Dejerine Sottas Disease
Dejerine Sottas Neuropathy
Dejerine Sottas Syndrome
Dejerine-Sottas Disease
Dejerine-Sottas Hypertrophic Neuropathy
Dejerine-Sottas Neuropathy
Dejerine-Sottas Syndrome
Disease, Dejerine-Sottas
HMSN
HMSN Type III
HMSN Type IIIs
HMSN Type VII
HMSN Type VIIs
HMSN3
Herditary Sensory and Motor Neuropathy
Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathy
Hereditary Motor and Sensory Neuropathy 3
Hereditary Motor and Sensory Neuropathy Type III
Hereditary, Type III, Motor and Sensory Neuropathy
Hereditary, Type VII, Motor and Sensory Neuropathy
Hypertrophic Neuropathy of Dejerine Sottas
Hypertrophic Neuropathy of Dejerine-Sottas
Neuropathies, Hereditary Motor and Sensory
Neuropathy, Dejerine-Sottas
Syndrome, Dejerine-Sottas
Type VII, HMSN  
Tree Number:   C10.500.300
C10.574.500.495
C10.668.829.800.300
C16.131.666.300
C16.320.400.375
Definition English:   A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343) 
Indexing Annotation English:   do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES
History Note English:   2000(1989) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   23777 
Unique Identifier:   D015417 

Occurrence in VHL: 		 

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