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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 
Autosomal Recessive Peripheral Neuropathy with or without Impaired Intellectual Development  
axonal neuropathy +   
brachial plexus neuropathy +   
Canavan disease  
Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome  
Cerebrocortical Degeneration of Infancy 
childhood spinal muscular atrophy +   
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  
familial episodic pain syndrome +   
Familial Partial Lipodystrophy Type 7  
Familial Visceral Neuropathy +   
Gerstmann-Straussler-Scheinker syndrome  
Gilles de la Tourette syndrome +   
Hereditary Central Nervous System Demyelinating Diseases +   
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  
mitochondrial DNA depletion syndrome 6  
mononeuropathy +   
motor peripheral neuropathy +   
A neuropathy that is characterized by inflammation or degeneration of the peripheral motor nerves. (DO)
myotonia congenita +   
myotonic dystrophy type 1 +   
neuritis +   
neuroacanthocytosis +   
neurofibromatosis +   
neurogenic scapuloperoneal syndrome Kaeser type  
neuromuscular disease +   
neuronal ceroid lipofuscinosis +   
Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine 
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Opticocochleodentate Degeneration 
Painful Neuropathy  
pantothenate kinase-associated neurodegeneration +   
PCWH syndrome  
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
primary cerebellar degeneration +   
Progressive Psychomotor Deterioration  
sensory peripheral neuropathy  
spinal muscular atrophy with predominant lower extremity +   
Spongiform Encephalopathy with Neuropsychiatric Features  
syndromic microphthalmia 10 
tuberous sclerosis +   
Unverricht-Lundborg syndrome +   
Wilson disease +   
X-Linked Intellectual Developmental Disorders +   

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 motor and sensory neuropathy, type VII ;   hereditary sensory and motor neuropathy ;   neuropathic muscular atrophy
Narrow Synonyms: sensory neuropathy with spastic paraplegia
Primary IDs: MESH:D015417
Definition Sources: https://www.ninds.nih.gov/health-information/disorders/peripheral-neuropathy "DO" "DO"

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