You have selected the view in English
| Descriptor English: | Hereditary Sensory and Motor Neuropathy | ||||||
| Descriptor Spanish: |
Neuropatía Hereditaria Motora y Sensorial
| ||||||
| Descriptor Portuguese: | Neuropatia Hereditária Motora e Sensorial | ||||||
| Descriptor 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 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D015417 | ||||||
| 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 |
||||||
| Previous Indexing: |
Charcot-Marie Disease (1975-1988) Muscular Atrophy (1972-1988) Neuromuscular Diseases (1979-1988) |
||||||
| Public MeSH Note: | 2000; see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1988-1999 |
||||||
| History Note: | 2000(1989) |
||||||
| DeCS ID: | 23777 | ||||||
| Unique ID: | D015417 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1988/01/01 | ||||||
| Date of Entry: | 1999/11/08 | ||||||
| Revision Date: | 2018/06/30 |
|
|
Hereditary Sensory and Motor Neuropathy
- Preferred
Hereditary, Type VII, Motor and Sensory Neuropathy
- Narrower
HMSN Type III
- Related but not broader or narrower
| 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 |
| Concept UI |
M0336471 |
| Preferred term | Hereditary, Type VII, Motor and Sensory Neuropathy |
| Entry term(s) |
HMSN Type VII HMSN Type VIIs Type VII, HMSN |
| 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 |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
