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Ontology Browser
Term:
Subacute Combined Degeneration (DOID:9007110)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
aceruloplasminemia  
agenesis of the corpus callosum with peripheral neuropathy  
amyotrophic lateral sclerosis +   
baylisascariasis 
Boylan Dew Greco Syndrome 
BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS  
CAMFAK Syndrome 
central pontine myelinolysis  
Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy  
Childhood-onset Neurodegeneration with Ataxia, Tremor, Optic Atrophy, and Cognitive Decline  
Childhood-Onset Neurodegeneration with Brain Atrophy  
Childhood-Onset Neurodegeneration with Cerebellar Atrophy  
Chronic Traumatic Encephalopathy 
congenital intrinsic factor deficiency  
Demyelinating Autoimmune Diseases, CNS +   
demyelinating disease +   
epidural abscess 
eye degenerative disease +   
eyelid degenerative disease +  
Feigenbaum Bergeron Richardson Syndrome 
FINCA Syndrome  
Groll Hirschowitz Syndrome 
Hamano Tsukamoto Syndrome 
hereditary ataxia +   
Hereditary Central Nervous System Demyelinating Diseases +   
Huntington's disease-like 2  
Hypotonia, Congenital Nystagmus, Ataxia and Abnormal Auditory Brainstem Response 
Idiopathic Basal Ganglia Calcification 1  
Idiopathic Basal Ganglia Calcification 6  
Idiopathic Basal Ganglia Calcification 7  
Imerslund-Grasbeck Syndrome +   
LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME  
Marchiafava-Bignami Disease 
methylmalonic aciduria and homocystinuria type cblC  
motor neuron disease +   
multiple system atrophy +   
myelitis +   
myelomeningocele +   
myoclonic cerebellar dyssynergia +  
Nervous System Heredodegenerative Disorders +   
Nervous System Paraneoplastic Syndromes +   
neurodegeneration with brain iron accumulation +   
NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA  
NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE  
Neurodevelopmental Disorder with Epilepsy, Spasticity, and Brain Atrophy  
Neuronal Intranuclear Inclusion Disease  
neuroschistosomiasis 
olivopontocerebellar atrophy +   
Ophthalmoplegic Migraine 
PEHO syndrome  
pernicious anemia +   
plexopathy 
Pneumorrhachis 
polyradiculoneuropathy +   
pontocerebellar hypoplasia +   
postpoliomyelitis syndrome 
primary cerebellar degeneration +   
prion disease +   
progressive multifocal leukoencephalopathy 
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant 
Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression  
Retrograde Degeneration  
secondary Parkinson disease +   
SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS  
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal 
Spastic Pseudosclerosis 
Spinal Cord Injuries +   
Spinal Cord Neoplasms +   
Spinal Cord Vascular Diseases +   
Spinal Intradural Arachnoid Cysts 
spinal muscular atrophy +   
Stiff-Person syndrome  
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
Striatal Degeneration, Autosomal Dominant +   
Subacute Cerebellar Degeneration 
Subacute Combined Degeneration  
A neuropathy due to VITAMIN B 12 DEFICIENCY or to excessive NITROUS OXIDE inhalation. It is associated with overproduction of the myelinolytic TUMOR NECROSIS FACTOR-ALPHA.
synucleinopathy +   
syringomyelia +   
tabes dorsalis +  
tauopathy +   
TDP-43 Proteinopathies +   
tertiary neurosyphilis +  
tethered spinal cord syndrome 
Thiamine Metabolism Dysfunction Syndrome 4 (Bilateral Striatal Degeneration and Progressive Polyneuropathy Type)  
transcobalamin II deficiency  
vascular myelopathy 
Wallerian Degeneration +   

Synonyms
Exact Synonyms: Subacute Combined Neuropathy Degeneration
Primary IDs: MESH:D052879 ;   RDO:0007600
Definition Sources: MESH:D052879

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