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Descriptor in English: Hereditary Sensory and Motor Neuropathy
Descriptor in Spanish: Neuropatía Hereditaria Motora y Sensorial
Descriptor in Portuguese: Neuropatia Hereditária Motora e Sensorial
Descriptor in French: Neuropathie héréditaire motrice et sensitive
Entry term(s): 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(s): C10.500.300
C10.574.500.495
C10.668.829.800.300
C16.131.666.300
C16.320.400.375
Scope note: 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)
Annotation: do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
History Note: 2000(1989)
DeCS UI: 23777
Descriptor UI: D015417
Date Established: 1988/01/01
Date of Entry: 1999/11/08
Revision Date: 2018/06/30
Hereditary Sensory and Motor Neuropathy - Preferred
Concept UI M0023767
Scope note 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)
Preferred term Hereditary Sensory and Motor Neuropathy
Entry term(s) HMSN
Herditary Sensory and Motor Neuropathy
Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathy
Neuropathies, Hereditary Motor and Sensory
Hereditary, Type VII, Motor and Sensory Neuropathy - Narrower
Concept UI M0336471
Preferred term Hereditary, Type VII, Motor and Sensory Neuropathy
Entry term(s) HMSN Type VII
HMSN Type VIIs
Type VII, HMSN
HMSN Type III - Related but not broader or narrower
Concept UI M0023764
Preferred term HMSN Type III
Entry term(s) 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 Type IIIs
HMSN3
Hereditary Motor and Sensory Neuropathy 3
Hereditary Motor and Sensory Neuropathy Type III
Hereditary, Type III, Motor and Sensory Neuropathy
Hypertrophic Neuropathy of Dejerine Sottas
Hypertrophic Neuropathy of Dejerine-Sottas
Neuropathy, Dejerine-Sottas
Syndrome, Dejerine-Sottas



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