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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
neuropathy +     
agenesis of the corpus callosum with peripheral neuropathy  
autoimmune disease of musculoskeletal system +   
autonomic peripheral neuropathy 
axonal neuropathy +   
bone disease +   
brachial plexus neuropathy +   
cartilage disease +   
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME  
connective tissue disease +   
cranial nerve disease +   
diabetic neuropathy +   
erythromelalgia  
fasciitis +  
Foot Deformities +   
Foot Diseases +   
Hand Deformities +   
hereditary neuropathy with liability to pressure palsies  
hereditary sensory neuropathy +   
inflammatory and toxic neuropathy +   
ischemic neuropathy 
Jaw Diseases +   
Joint Diseases +   
mononeuropathy +   
motor peripheral neuropathy +   
muscular disease +   
Musculoskeletal Abnormalities +   
musculoskeletal system benign neoplasm +   
musculoskeletal system cancer +   
neuritis +   
neuromuscular disease +   
A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA.
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT  
sensory peripheral neuropathy  

Synonyms
Exact Synonyms: Amyotonia Congenita ;   Benign Fasciculation-Cramp Syndrome ;   Benign Fasciculation-Cramp Syndromes ;   Cramp Fasciculation Syndrome ;   Cramp-Fasciculation Syndromes ;   Foley Denny Brown Syndrome ;   Oppenheim Disease ;   Oppenheim's Disease ;   Oppenheims Disease ;   neuromuscular diseases
Primary IDs: MESH:D009468
Alternate IDs: RDO:0001720
Xrefs: OMIM:PS605253
Definition Sources: MESH:D009468, http://www.nlm.nih.gov/medlineplus/neuromusculardisorders.html

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