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Medical Subject Headings
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/MESH/D015417
http://purl.bioontology.org/ontology/MESH/D015417
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|---|---|
| Preferred Name | Hereditary Sensory and Motor Neuropathy |
| Definitions |
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)
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| Synonyms |
Dejerine Sottas Disease
Hereditary, Type VII, Motor and Sensory Neuropathy
Proximal Hereditary Motor Neuropathy Type I
Dejerine Sottas Neuropathy
HMSN Type VIIs
Syndrome, Dejerine-Sottas
Hereditary Motor and Sensory Neuropathy
Dejerine-Sottas Syndrome
Dejerine-Sottas Neuropathy
Hereditary Motor and Sensory Neuropathy 3
HMSN Type IIIs
HMSN Type VII
Hereditary Motor and Sensory Neuropathies
Dejerine-Sottas Disease
Neuropathy, Dejerine-Sottas
Type VII, HMSN
Charcot-Marie-Tooth Disease, Type 3
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
HMSN Type III
Dejerine-Sottas Hypertrophic Neuropathy
Hereditary Motor and Sensory Neuropathy Type III
HMSN3
HMSN
Hypertrophic Neuropathy of Dejerine Sottas
Hypertrophic Neuropathy of Dejerine-Sottas
Dejerine Sottas Syndrome
Hereditary, Type III, Motor and Sensory Neuropathy
Disease, Dejerine-Sottas
Charcot Marie Tooth Disease, Type 3
Herditary Sensory and Motor Neuropathy
Neuropathies, Hereditary Motor and Sensory
CMT4f
HMN (Hereditary Motor Neuropathy) Proximal Type I
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | 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) |
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| altLabel |
Dejerine Sottas Disease
Hereditary, Type VII, Motor and Sensory Neuropathy
Proximal Hereditary Motor Neuropathy Type I
Dejerine Sottas Neuropathy
HMSN Type VIIs
Syndrome, Dejerine-Sottas
Hereditary Motor and Sensory Neuropathy
Dejerine-Sottas Syndrome
Dejerine-Sottas Neuropathy
Hereditary Motor and Sensory Neuropathy 3
HMSN Type IIIs
HMSN Type VII
Hereditary Motor and Sensory Neuropathies
Dejerine-Sottas Disease
Neuropathy, Dejerine-Sottas
Type VII, HMSN
Charcot-Marie-Tooth Disease, Type 3
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
HMSN Type III
Dejerine-Sottas Hypertrophic Neuropathy
Hereditary Motor and Sensory Neuropathy Type III
HMSN3
HMSN
Hypertrophic Neuropathy of Dejerine Sottas
Hypertrophic Neuropathy of Dejerine-Sottas
Dejerine Sottas Syndrome
Hereditary, Type III, Motor and Sensory Neuropathy
Disease, Dejerine-Sottas
Charcot Marie Tooth Disease, Type 3
Herditary Sensory and Motor Neuropathy
Neuropathies, Hereditary Motor and Sensory
CMT4f
HMN (Hereditary Motor Neuropathy) Proximal Type I
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| prefLabel | Hereditary Sensory and Motor Neuropathy
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| Machine permutation | 2000; see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1988-1999, for HMN (HEREDITARY MOTOR NEUROPATHY) PROXIMAL TYPE I see SPINAL MUSCULAR ATROPHIES OF CHILDHOOD 1988-2025,
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| HN | 2000(1989); for HMN (HEREDITARY MOTOR NEUROPATHY) PROXIMAL TYPE I use SPINAL MUSCULAR ATROPHIES OF CHILDHOOD 1988-2025
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| Mapped from |
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| type | |
| tui | T047
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| TERMUI |
T755169
T745673
T045523
T371177
T370514
T001146884
T817093
T769515
T045522
T811481
T045519
T371167
T811486
T817092
T045518
T045524
T811480
T817094
T045521
T817089
T811482
T370515
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| TH |
OMIM (2013)
NLM (2000)
UNK (19XX)
NLM (2013)
NLM (2010)
NLM (1988)
NLM (2011)
ORD (2010)
NLM (2025)
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| MMR | 20260101
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| notation | D015417
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| Semantic type UMLS property | |
| Inverse of AQ |
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| DX | 19880101
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| cui |
C0027888
C0011195
C0043116
C0019816
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| DC | 1
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| MN |
C10.574.500.495
C10.668.829.800.300
C10.500.300
C16.131.666.300
C16.320.400.375
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| AN | do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES
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| AQL | BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
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| MDA | 20090722
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| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |