Send us a Message



 Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) RatMine GViewer (Genome Viewer) Overgo Probe Designer ACP Haplotyper
Aging & Age-Related Disease Cancer Cardiovascular Disease COVID-19 Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models PhenoMiner (Quantitative Phenotypes) Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Poster Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Accessory Deep Peroneal Nerve 
Acrodynia 
agenesis of the corpus callosum with peripheral neuropathy  
Amyloid Neuropathies +   
Apical Hypertrophic Cardiomyopathy and Neuropathy  
autoimmune disease of peripheral nervous system +   
autonomic nervous system disease +   
autonomic peripheral neuropathy 
Autosomal Recessive Peripheral Neuropathy with or without Impaired Intellectual Development  
axonal neuropathy +   
brachial plexus neuropathy +   
Cataract Ataxia Deafness 
Cauda equina syndrome 
Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome  
complex regional pain syndrome +  
Congenital Myopathy with Neuropathy and Deafness  
Congenital Pain Insensitivity +   
cranial nerve disease +   
diabetic neuropathy +   
erythromelalgia  
familial episodic pain syndrome +   
Gamstorp-Wohlfart syndrome  
Hand-Arm Vibration Syndrome 
Harel-Yoon Syndrome  
Hereditary Motor Neuropathy with Myopathic Features  
hereditary sensory neuropathy +   
Hypertrophic Neuropathy and Cataract 
inflammatory and toxic neuropathy +   
Inherited Peripheral Neuropathy +   
Intellectual Developmental Disorder with Speech Delay and Axonal Peripheral Neuropathy  
ischemic neuropathy 
leprosy +   
lumbosacral plexus lesion 
mitochondrial DNA depletion syndrome 6  
mononeuropathy +   
Disease or trauma involving a single peripheral nerve in isolation, or out of proportion to evidence of diffuse peripheral nerve dysfunction. Mononeuropathy multiplex refers to a condition characterized by multiple isolated nerve injuries. Mononeuropathies may result from a wide variety of causes, including ISCHEMIA; traumatic injury; compression; CONNECTIVE TISSUE DISEASES; CUMULATIVE TRAUMA DISORDERS; and other conditions.
motor peripheral neuropathy +   
nerve compression syndrome +   
Neuralgia +   
neuritis +   
neuromuscular disease +   
neuropathy +   
Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine 
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Painful Neuropathy  
Peripheral Nerve Injuries  
peripheral nervous system neoplasm +   
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
polyneuropathy +   
radiculopathy +   
Sacral Plexopathy 
sensory peripheral neuropathy  
Small Fiber Neuropathy  
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy 
Tarlov Cysts 

Synonyms
Exact Synonyms: mononeuropathies ;   mononeuropathy multiplex syndrome ;   mononeuropathy multiplex syndromes
Primary IDs: MESH:D020422
Alternate IDs: RDO:0007406
Xrefs: ICD10CM:G58.9
Definition Sources: https://medlineplus.gov/ency/article/000780.htm "DO" "DO", MESH:D020422

paths to the root