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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
central nervous system disease +     
Paralysis +     
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY  
autoimmune disease of central nervous system +   
Autosomal Recessive Syndrome of Syndactyly, Undescended Testes and Central Nervous System Defects  
brain disease +   
Central Nervous System Infections +   
Central Nervous System Neoplasms +   
encephalomyelitis +   
endocrine-cerebro-osteodysplasia syndrome  
epidural abscess 
facial paralysis +   
Flynn Aird Syndrome 
gastroparesis +   
hemiplegia +   
high pressure neurological syndrome 
hyperekplexia +   
intracranial abscess 
maturity-onset diabetes of the young type 5  
meningitis +   
movement disease +   
neurodegenerative disease +   
neuronitis 
neurosarcoidosis +  
ocular motility disease +   
ophthalmoplegia +   
paraplegia +   
Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness.
Pneumocephalus 
pseudobulbar palsy +   
quadriplegia +   
Respiratory Paralysis 
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal  
spinal cord disease +   
Vocal Cord Paralysis +   

Synonyms
Exact Synonyms: Ataxic Paraplegia ;   Cerebral Paraplegia ;   Cerebral Paraplegias ;   Flaccid Paraplegia ;   Flaccid Paraplegias ;   Paralysis, Legs ;   Paralysis, Lower Extremities ;   Paralysis, Lower Limbs ;   Paraplegias ;   Spastic Paraplegia ;   Spastic Paraplegias ;   Spinal Paraplegia ;   ataxic paraplegias ;   lower paraplegia ;   spinal paraplegias
Primary IDs: MESH:D010264
Xrefs: EFO:0009679 ;   GARD:7327 ;   ICD10CM:G82.2 ;   ICD9CM:344.1 ;   NCI:C50687
Definition Sources: MESH:D010264

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