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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
agenesis of the corpus callosum with peripheral neuropathy  
Alexander Disease  
autonomic peripheral neuropathy 
axonal neuropathy +   
brachial plexus neuropathy +   
Canavan disease  
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME  
Cerebrocortical Degeneration of Infancy 
Cockayne syndrome +   
Congenital Muscular Dystrophy with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers 
cranial nerve disease +   
diabetic neuropathy +   
Dystonia Musculorum Deformans +   
erythromelalgia  
Familial Amyloid Polyneuropathies +   
familial encephalopathy with neuroserpin inclusion bodies  
Gerstmann-Straussler-Scheinker syndrome  
Gilles de la Tourette syndrome +   
Hereditary Central Nervous System Demyelinating Diseases +   
hereditary neuropathy with liability to pressure palsies  
Hereditary Optic Atrophies +   
hereditary sensory neuropathy +   
Huntington's disease +   
Huntington's disease-like 2  
Huntington's Disease-Like Syndrome  
inflammatory and toxic neuropathy +   
ischemic neuropathy 
Kennedy's disease  
Lafora disease  
Leukoencephalomyelopathy  
Lipodystrophy with Congenital Cataracts and Neurodegeneration  
Mental Retardation, X-Linked +   
Microphthalmia, Syndromic 10 
mitochondrial DNA depletion syndrome 6  
mononeuropathy +   
motor peripheral neuropathy +   
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)
myotonia congenita +   
myotonic dystrophy type 1 +   
neuritis +   
neuroacanthocytosis +   
neurofibromatosis +   
Neurogenic Scapuloperoneal Syndrome, Kaeser Type  
neuromuscular disease +   
neuronal ceroid lipofuscinosis +   
Opticocochleodentate Degeneration 
pantothenate kinase-associated neurodegeneration +   
PCWH syndrome  
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT  
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
primary cerebellar degeneration +   
sensory peripheral neuropathy  
Spinal Muscular Atrophy, Lower Extremity-Predominant, 2A, Autosomal Dominant  
Spinal Muscular Atrophy, Lower Extremity-Predominant, 2B, Autosomal Dominant  
Spongiform Encephalopathy with Neuropsychiatric Features  
survival motor neuron spinal muscular atrophy +   
tuberous sclerosis +   
Unverricht-Lundborg syndrome +   
Wilson disease +   

Synonyms
Exact Synonyms: HMSN ;   HMSN Type VII ;   HSMN ;   HSMN - Hereditary sensory and motor neuropathy ;   Herditary Sensory and Motor Neuropathy ;   Hereditary Motor and Sensory Neuropathies ;   Hereditary Sensory and Motor Neuropathy ;   Hereditary, Type VII, Motor and Sensory Neuropathy ;   neuropathic muscular atrophy
Narrow Synonyms: SENSORY NEUROPATHY WITH SPASTIC PARAPLEGIA
Primary IDs: MESH:D015417
Alternate IDs: RDO:0000988
Definition Sources: MESH:D015417

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