hereditary sensory and motor neuropathy

Preferred Label : hereditary sensory and motor neuropathy;

MeSH 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);

MeSH synonym : hmsn; herditary sensory and motor neuropathy; neuropathies, hereditary motor and sensory; Hereditary Motor and Sensory Neuropathies; hereditary motor and sensory neuropathy;

CISMeF acronym : HSMN;

MeSH hyponym : hereditary, type VII, motor and sensory neuropathy; HMSN Type VII; HMSN Type VIIs; Type VII, HMSN; Proximal Hereditary Motor Neuropathy Type I;

Related MeSH term : 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;

MeSH annotation : do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; DF: NEUROPATHIES HEREDITARY MOTOR SENSORY; do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES;

Wikipedia link : https://en.wikipedia.org/wiki/Hereditary motor and sensory neuropathies;

Details

Origin ID

D015417;

UMLS CUI

C0027888;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Charcot-Marie-Tooth disease type 3 [DO Concept]
- Charcot-Marie-Tooth disease type 4 [DO Concept]
- Charcot-Marie-Tooth disease type 4F [ORDO Disease]
- Charcot-marie-tooth disease, demyelinating, type 1b [OMIM Phenotype]
- Charcot-marie-tooth disease, demyelinating, type 1d [OMIM Phenotype]
- Charcot-marie-tooth disease, demyelinating, type 4f [OMIM Phenotype]
- Dejerine-Sottas neuropathy [PASCAL descriptor]
- Dejerine-Sottas syndrome [ICD-11 More detail]
- Dejerine-Sottas syndrome [ORDO Disease]
- Déjérine-Sottas disease (disorder) [SNOMED CT concept]
- Hereditary motor and sensory neuropathy V [OMIM Phenotype]
- Hereditary motor and sensory neuropathy with retinitis pigmentosa (disorder) [SNOMED CT concept]
- Hereditary neuropathy with liability to pressure palsies [ORDO Disease]
- Hypertrophic neuropathy of dejerine-sottas [OMIM Phenotype]
- Tomaculous neuropathy [PASCAL descriptor]
- Tomaculous neuropathy [MedDRA LLT]
- dejerine-sottas disease [SNOMED Notion]
- motor peripheral neuropathy [DO Concept]
Currated CISMeF NLP mapping
- Charcot-Marie-Tooth Disease [NCIt concept]
- Charcot-Marie-Tooth disease [MedDRA LLT]
- Charcot-Marie-Tooth disease (disorder) [Inactive SNOMED CT concept]
- Hereditary motor and sensory neuropathy [ICD-10 Sub-category]
- Hereditary motor and sensory neuropathy [ICD-11 Category]
- Hereditary motor and sensory neuropathy [ICD-10 Sub-category (who)]
- Hereditary motor and sensory neuropathy [MedDRA Preferred Term]
- Hereditary motor and sensory neuropathy [ORDO Disease]
- Hereditary motor and sensory neuropathy (disorder) [SNOMED CT concept]
- charcot-marie-tooth disease [MedlinePlus Topic]
- hereditary motor sensory neuropathy [Disease (Nov.)]
- peroneal muscular atrophy [SNOMED Notion]
DO Cross reference
- motor peripheral neuropathy [DO Concept]
Manual NTBT mappings (CISMeF)
- Autosomal dominant hereditary axonal motor and sensory neuropathy [ORDO Disease]
- Autosomal dominant hereditary demyelinating motor and sensory neuropathy [ORDO Disease]
- Autosomal dominant intermediate Charcot-Marie-Tooth disease [ORDO Disease]
- Autosomal recessive axonal hereditary motor and sensory neuropathy [ORDO Disease]
- Autosomal recessive hereditary demyelinating motor and sensory neuropathy [ORDO Disease]
- Autosomal recessive intermediate Charcot-Marie-Tooth disease type A [ORDO Disease]
- Genetic peripheral neuropathy [ORDO Disease]
- Hereditary motor and sensory neuropathy with acrodystrophy [ORDO Disease]
- Rare peripheral neuropathy [ORDO Disease]
- Severe early-onset axonal neuropathy due to MFN2 deficiency [ORDO Disease]
- X-linked Charcot-Marie-Tooth disease type 1 [ORDO Disease]
- X-linked recessive hereditary axonal motor and sensory neuropathy [ORDO Disease]
Ne pas confondre avec
- hereditary sensory and autonomic neuropathies [MeSH Descriptor]
ORDO relation(s)
- Hereditary motor and sensory neuropathy [ORDO Disease]
Record concept(s)
- HMN (Hereditary motor neuropathy) proximal type I [MeSH concept]
- HMSN type III [MeSH concept]
- hereditary sensory and motor neuropathy [MeSH concept]
- hereditary, type VII, motor and sensory neuropathy [MeSH concept]
Related MeSH Supplementary Concept(s)
- cardioneuromyopathy with hyaline masses and nemaline rods [MeSH Supplementary Concept]
- hagemoser weinstein bresnick syndrome [MeSH Supplementary Concept]
- hereditary motor and sensory neuropathy VI [MeSH Supplementary Concept]
- hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy [MeSH Supplementary Concept]
- neuropathy, distal hereditary motor, type VIIA [MeSH Supplementary Concept]
- neuropathy, hereditary motor and sensory, okinawa type [MeSH Supplementary Concept]
- neuropathy, hereditary motor and sensory, russe type [MeSH Supplementary Concept]
- neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive [MeSH Supplementary Concept]
- neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance [MeSH Supplementary Concept]
- neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive [MeSH Supplementary Concept]
- neuropathy, hereditary thermosensitive [MeSH Supplementary Concept]
- polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive [MeSH Supplementary Concept]
- sensory ataxic neuropathy, dysarthria, and ophthalmoparesis [MeSH Supplementary Concept]
- slowed nerve conduction velocity, autosomal dominant [MeSH Supplementary Concept]
- spastic paraplegia, optic atrophy, and neuropathy [MeSH Supplementary Concept]
- tamari goodman syndrome [MeSH Supplementary Concept]
- tomaculous neuropathy [MeSH Supplementary Concept]
- tremor hereditary essential, 2 [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- hereditary sensory and autonomic neuropathies [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary motor and sensory neuropathy [ORDO Disease]
- Hereditary motor and sensory neuropathy [ICD-10 Sub-category (who)]
- Hereditary motor and sensory neuropathy [ICD-10 Sub-category]
- Hereditary motor and sensory neuropathy [MedDRA Preferred Term]
- Hereditary motor and sensory neuropathy (disorder) [SNOMED CT concept]
- Neuropathic muscular atrophy [MedDRA Preferred Term]
- motor peripheral neuropathy [DO Concept]
Validated automatic mappings to BTNT
- Charcot Marie Tooth disease [Disease (Nov.)]
- Charcot-Marie-Tooth disease type 4F [DO Concept]
- Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy [ORDO Disease]
- Dejerine-Sottas Neuropathy [NCIt concept]
- hereditary motor and sensory neuropathy Is [Disease (Nov.)]
- hereditary motor and sensory polyneuropathy type III [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients