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Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain (DOID:9006631)
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Parent Terms Term With Siblings Child Terms
Abetalipoproteinemia Neuropathy  
Accessory Deep Peroneal Nerve 
adult-onset ataxia and polyneuropathy  
agenesis of the corpus callosum with peripheral neuropathy  
Alexander Disease  
Amyloid Neuropathies +   
Apical Hypertrophic Cardiomyopathy and Neuropathy  
Arts syndrome  
Ataxia with Fasciculations 
Ataxia with Myoclonic Epilepsy and Presenile Dementia 
Ataxia, Deafness, and Cardiomyopathy 
Ataxia-Microcephaly-Cataract Syndrome 
Ataxia-Oculomotor Apraxia 4  
ataxic cerebral palsy 
Atonic-Astatic Syndrome of Foerster 
autoimmune disease of peripheral nervous system +   
autonomic nervous system disease +   
Bangstad Syndrome 
Behr syndrome  
Benign Childhood Paroxysmal Tonic Upgaze with Ataxia 
Bhaskar Jagannathan Syndrome 
Canavan disease  
CANOMAD Syndrome 
Carnitine Acetyltransferase Deficiency  
Cataract Ataxia Deafness 
Cataracts, Ataxia, Short Stature, and Mental Retardation 
Cauda equina syndrome 
Cerebrocortical Degeneration of Infancy 
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
childhood spinal muscular atrophy +   
Christianson syndrome  
COACH syndrome  
Cockayne syndrome +   
coenzyme Q10 deficiency disease +   
complex regional pain syndrome +  
Congenital Muscular Dystrophy with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers 
Congenital Myopathy with Neuropathy and Deafness  
Congenital Pain Insensitivity +   
Deafness Hyperuricemia Neurologic Ataxia 
diabetic neuropathy +   
Dystonia Musculorum Deformans +   
Erythrokeratodermia with Ataxia 
Familial Amyloid Polyneuropathies +   
familial encephalopathy with neuroserpin inclusion bodies  
familial isolated deficiency of vitamin E  
Gait Ataxia +   
Gamstorp-Wohlfart syndrome  
Gerstmann-Straussler-Scheinker syndrome  
Gilles de la Tourette syndrome +   
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine  
Hand-Arm Vibration Syndrome 
Harel-Yoon Syndrome  
hereditary ataxia +   
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  
Hypertrophic Neuropathy and Cataract 
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
Hypotonia, Congenital Nystagmus, Ataxia and Abnormal Auditory Brainstem Response 
Inherited Peripheral Neuropathy  
Joubert syndrome 7  
Kennedy's disease  
Lafora disease  
leprosy +   
Leukoencephalopathy with Ataxia  
Lipodystrophy with Congenital Cataracts and Neurodegeneration  
lumbosacral plexus lesion 
Mental Retardation, X-Linked +   
mitochondrial DNA depletion syndrome 6  
Mitochondrial Myopathy, and Ataxia  
mononeuropathy +   
motor peripheral neuropathy +   
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
Myokymia 1  
myotonia congenita +   
myotonic dystrophy type 1 +   
nerve compression syndrome +   
Neuralgia +   
neuritis +   
neuroacanthocytosis +   
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia   
neurofibromatosis +   
neurogenic scapuloperoneal syndrome Kaeser type  
neuronal ceroid lipofuscinosis +   
neuropathy +   
Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine 
optic atrophy 10  
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Opticocochleodentate Degeneration 
Painful Neuropathy  
pantothenate kinase-associated neurodegeneration +   
Partington syndrome  
PCWH syndrome  
Peripheral Nerve Injuries  
peripheral nervous system neoplasm +   
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
PHARC syndrome  
polyneuropathy +   
Posterior Column Ataxia with Retinitis Pigmentosa  
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
primary cerebellar degeneration +   
progressive myoclonus epilepsy 1B  
Progressive Psychomotor Deterioration  
radiculopathy +   
Reardon Wilson Cavanagh Syndrome 
Richards-Rundle Syndrome 
Sacral Plexopathy 
Sensory Ataxia, Autosomal Dominant  
Small Fiber Neuropathy  
Spastic Ataxia with Congenital Miosis 
Spastic Paraplegia, Ataxia, and Mental Retardation 
spinal muscular atrophy with lower extremity predominance +   
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy 
Spinocerebellar Ataxias +   
spondyloepimetaphyseal dysplasia, Genevieve-type  
Spongiform Encephalopathy with Neuropsychiatric Features  
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
syndromic microphthalmia 10 
Tapetoretinal Degeneration with Ataxia 
Tarlov Cysts 
Treft Sanborn Carey Syndrome 
Tremor of Intention, Ataxia, and Lipofuscinosis 
Tryptophanuria with Dwarfism 
tuberous sclerosis +   
Unverricht-Lundborg syndrome +   
Wilson disease +   

Primary IDs: MESH:C564894 ;   RDO:0013705

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.