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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
alpha-methylacyl-CoA racemase deficiency  
autoimmune disease of central nervous system +   
autoimmune disease of the nervous system +   
autonomic nervous system disease +   
Autosomal Recessive Syndrome of Syndactyly, Undescended Testes and Central Nervous System Defects  
BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME  
brain disease +   
central nervous system disease +   
Central Nervous System Infections +   
Central Nervous System Neoplasms +   
Chronobiology Disorders +   
Congenital Cataracts, Facial Dysmorphism, and Neuropathy  
congenital nervous system abnormality +   
diplegia of upper limb 
encephalomyelitis +   
endocrine-cerebro-osteodysplasia syndrome  
epidural abscess 
Flynn Aird Syndrome 
Gerstmann syndrome 
hemiplegia +   
herpes zoster +   
high pressure neurological syndrome 
hyperekplexia +   
Infantile Multisystem Neurologic Disease with Osseous Fragility 
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease +   
intestinal pseudo-obstruction +   
intracranial abscess 
LETM1-ASSOCIATED CLINICAL SPECTRUM WITH PREDOMINANT NERVOUS SYSTEM INVOLVEMENT  
maturity-onset diabetes of the young type 5  
meningitis +   
movement disease +   
Nerve Injuries +   
Nervous System Malformations +   
Nervous System Neoplasms +   
Nervous System Trauma +   
Neurocutaneous Syndromes +   
neurodegenerative disease +   
A central nervous system disease that results in the progressive deterioration of function or structure of neurons. (DO)
Neurologic Manifestations +   
neuronitis 
neurosarcoidosis +  
Norrie disease  
ocular motility disease +   
paraplegia +   
peripheral nervous system disease +   
Pneumocephalus 
Polyglucosan Body Disease, Adult Form  
quadriplegia +   
Roy Maroteaux Kremp Syndrome 
sensory system disease +   
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal  
spinal cord disease +   
Tang Hsi Ryu Syndrome 
toxic encephalopathy +   
 aceruloplasminemia  
 agenesis of the corpus callosum with peripheral neuropathy  
 BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS  
 Childhood-onset Neurodegeneration with Ataxia, Tremor, Optic Atrophy, and Cognitive Decline  
 childhood-onset neurodegeneration with brain atrophy  
 Childhood-Onset Neurodegeneration with Cerebellar Atrophy  
 demyelinating disease +   
 eye degenerative disease +   
 Feigenbaum Bergeron Richardson Syndrome 
 FINCA Syndrome  
 hereditary ataxia +   
 Huntington's disease-like 2  
 Idiopathic Basal Ganglia Calcification 1  
 Idiopathic Basal Ganglia Calcification 6  
 Idiopathic Basal Ganglia Calcification 7  
 LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME  
 motor neuron disease +   
 multiple system atrophy +   
 myoclonic cerebellar dyssynergia +  
 Nervous System Heredodegenerative Disorders +   
 Nervous System Paraneoplastic Syndromes +   
 NEURODEGENERATION AND SEIZURES DUE TO COPPER TRANSPORT DEFECT  
 Neurodegeneration with Ataxia and Late-Onset Optic Atrophy  
 neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset  
 neurodegeneration with brain iron accumulation +   
 NEURODEGENERATION WITH DEVELOPMENTAL DELAY, EARLY RESPIRATORY FAILURE, MYOCLONIC SEIZURES, AND BRAIN ABNORMALITIES  
 NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATAXIA AND COGNITIVE DECLINE  
 NEURODEGENERATION, CHILDHOOD-ONSET, WITH MULTISYSTEM INVOLVEMENT DUE TO MITOCHONDRIAL DYSFUNCTION  
 NEURODEGENERATION, CHILDHOOD-ONSET, WITH PROGRESSIVE MICROCEPHALY  
 NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA  
 NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE  
 NEURODEGENERATION, INFANTILE-ONSET, WITH OPTIC ATROPHY AND BRAIN ABNORMALITIES  
 neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures  
 neuronal intranuclear inclusion disease  
 olivopontocerebellar atrophy +   
 PEHO syndrome  
 plexopathy 
 pontocerebellar hypoplasia +   
 postpoliomyelitis syndrome 
 primary cerebellar degeneration +   
 prion disease +   
 Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant 
 Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression  
 secondary Parkinson disease +   
 SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS  
 Spastic Pseudosclerosis 
 stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
 Subacute Combined Degeneration  
 synucleinopathy +   
 tauopathy +   
 TDP-43 Proteinopathies +   

Synonyms
Exact Synonyms: Degenerative Neurologic Disease ;   Degenerative Neurologic Disorder ;   Nervous System Degenerative Diseases ;   Neurodegenerative Diseases ;   Neurodegenerative Disorder ;   Neurodegenerative Disorders ;   central nervous system degenerative diseases ;   degenerative disease ;   degenerative neurologic diseases ;   degenerative neurologic disorders
Narrow Synonyms: Neurodegenerative illness progressing to crippling dystonia and death with relentless cerebral atrophy ;   progressive neurodegenerative disease ;   severe cystic degeneration of the brain ;   subacute myelo-opticoneuropathy
Broad Synonyms: TMEM63B-ASSOCIATED DISORDER
Primary IDs: MESH:D019636
Xrefs: EFO:0005772 ;   EFO:0020919 ;   ICD10CM:G31.9 ;   NCI:C27090
Definition Sources: http://en.wikipedia.org/wiki/Degenerative_disease "DO" "DO", http://en.wikipedia.org/wiki/Neurodegeneration "DO" "DO"

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