MeSH Browser

MeSH Heading: Hereditary Sensory and Motor Neuropathy
Tree Number(s): C10.500.300; C10.574.500.495; C10.668.829.800.300; C16.131.666.300; C16.320.400.375
Unique ID: D015417
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D015417
Annotation: do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES
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)
Entry Term(s): CMT4f; Charcot-Marie-Tooth Disease, Demyelinating, Type 4f; Charcot-Marie-Tooth Disease, Type 3; Dejerine-Sottas Disease; Dejerine-Sottas Neuropathy; Dejerine-Sottas Syndrome; HMSN; HMSN Type III; HMSN Type VII; 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; Neuropathies, Hereditary Motor and Sensory
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)
Date Established: 1988/01/01
Date of Entry: 1999/11/08
Revision Date: 2018/06/30

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Nervous System Diseases [C10]
- Nervous System Malformations [C10.500]

Nervous System Diseases [C10]
- Neurodegenerative Diseases [C10.574]
  - Heredodegenerative Disorders, Nervous System [C10.574.500]

Nervous System Diseases [C10]
- Neuromuscular Diseases [C10.668]
  - Peripheral Nervous System Diseases [C10.668.829]
    - Polyneuropathies [C10.668.829.800]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
  - Nervous System Malformations [C16.131.666]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Heredodegenerative Disorders, Nervous System [C16.320.400]

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)
Terms: Hereditary Sensory and Motor Neuropathy Preferred Term
Term UI T755169
Date07/22/2009
LexicalTag NON
ThesaurusID NLM (2010); Herditary Sensory and Motor Neuropathy
Term UI T750855
Date05/11/2009
LexicalTag NON
ThesaurusID; Hereditary Motor and Sensory Neuropathies
Term UI T045523
Date06/07/1988
LexicalTag NON
ThesaurusID UNK (19XX); Hereditary Motor and Sensory Neuropathy
Term UI T769515
Date04/15/2010
LexicalTag NON
ThesaurusID; Neuropathies, Hereditary Motor and Sensory
Term UI T045524
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1988); HMSN
Term UI T045522
Date06/07/1988
LexicalTag ABB
ThesaurusID

HMSN Type III Related

Hereditary, Type VII, Motor and Sensory Neuropathy Narrower

Hereditary Sensory and Motor Neuropathy MeSH Descriptor Data 2024