Hereditary Sensory and Motor Neuropathy

"Hereditary Sensory and Motor Neuropathy" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

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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)

Descriptor ID	D015417
MeSH Number(s)	C10.500.300 C10.574.500.495 C10.668.829.800.300 C16.131.666.300 C16.320.400.375
Concept/Terms	Hereditary Sensory and Motor Neuropathy Hereditary Sensory and Motor Neuropathy Neuropathies, Hereditary Motor and Sensory Hereditary Motor and Sensory Neuropathy HMSN Herditary Sensory and Motor Neuropathy Hereditary Motor and Sensory Neuropathies Hereditary, Type VII, Motor and Sensory Neuropathy Hereditary, Type VII, Motor and Sensory Neuropathy HMSN Type VII HMSN Type VIIs Type VII, HMSN HMSN Type III HMSN Type III HMSN Type IIIs Charcot-Marie-Tooth Disease, Type 3 Charcot Marie Tooth Disease, Type 3 CMT4f Dejerine-Sottas Disease Dejerine Sottas Disease Disease, Dejerine-Sottas Dejerine-Sottas Neuropathy Dejerine Sottas Neuropathy Neuropathy, Dejerine-Sottas Hereditary, Type III, Motor and Sensory Neuropathy HMSN3 Hereditary Motor and Sensory Neuropathy 3 Hypertrophic Neuropathy of Dejerine-Sottas Dejerine-Sottas Hypertrophic Neuropathy Hypertrophic Neuropathy of Dejerine Sottas Hereditary Motor and Sensory Neuropathy Type III Charcot-Marie-Tooth Disease, Demyelinating, Type 4f Dejerine-Sottas Syndrome Dejerine Sottas Syndrome Syndrome, Dejerine-Sottas

Below are MeSH descriptors whose meaning is more general than "Hereditary Sensory and Motor Neuropathy".

Diseases [C]
Nervous System Diseases [C10]
Nervous System Malformations [C10.500]
Hereditary Sensory and Motor Neuropathy [C10.500.300]
Neurodegenerative Diseases [C10.574]
Heredodegenerative Disorders, Nervous System [C10.574.500]
Hereditary Sensory and Motor Neuropathy [C10.574.500.495]
Neuromuscular Diseases [C10.668]
Peripheral Nervous System Diseases [C10.668.829]
Polyneuropathies [C10.668.829.800]
Hereditary Sensory and Motor Neuropathy [C10.668.829.800.300]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Nervous System Malformations [C16.131.666]
Hereditary Sensory and Motor Neuropathy [C16.131.666.300]
Genetic Diseases, Inborn [C16.320]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Hereditary Sensory and Motor Neuropathy [C16.320.400.375]

Below are MeSH descriptors whose meaning is related to "Hereditary Sensory and Motor Neuropathy".

Below are MeSH descriptors whose meaning is more specific than "Hereditary Sensory and Motor Neuropathy".

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