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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
amyotrophic lateral sclerosis +   
baylisascariasis 
epidural abscess 
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance 
lateral sclerosis  
motor neuritis +  
MOTOR NEURON ATROPHY +   
Motor Neuron Disease with Dementia and Ophthalmoplegia 
multisystem proteinopathy 
myelitis +   
myelomeningocele +   
neuroschistosomiasis 
nonparalytic poliomyelitis 
Pneumorrhachis 
poliomyelitis +   
primary cerebellar degeneration +   
Primary Lateral Sclerosis Juvenile  
progressive bulbar palsy +   
progressive muscular atrophy  
pseudobulbar palsy +   
Spinal Cord Injuries +   
Spinal Cord Neoplasms +   
Spinal Cord Vascular Diseases +   
Spinal Intradural Arachnoid Cysts 
spinal muscular atrophy +   
A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. (DO)
Stiff-Person syndrome  
Subacute Combined Degeneration  
syringomyelia +   
tabes dorsalis +  
tertiary neurosyphilis +  
tethered spinal cord syndrome 
vascular myelopathy 

Synonyms
Exact Synonyms: adult onset spinal muscular atrophy ;   bulbospinal neuronopathies ;   bulbospinal neuronopathy ;   distal spinal muscular atrophy ;   hereditary motor neuronopathies ;   hereditary motor neuronopathy ;   myelopathic muscular atrophy ;   oculopharyngeal spinal muscular atrophy ;   progressive myelopathic muscular atrophy ;   progressive proximal myelopathic muscular atrophy ;   spinal amyotrophies ;   spinal amyotrophy
Narrow Synonyms: proximal spinal muscular atrophy ;   spinal muscular atrophy, dominant
Primary IDs: MESH:D009134
Xrefs: GARD:7674 ;   ICD10CM:G12.9 ;   ICD9CM:335.1 ;   NCI:C85075
Definition Sources: http://en.wikipedia.org/wiki/Spinal_muscular_atrophy "DO", https://ghr.nlm.nih.gov/condition/spinal-muscular-atrophy "DO", https://www.ncbi.nlm.nih.gov/pubmed/26022173 "DO"

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