Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP 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 FTP 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 Genome Scanner
Aging & Age-Related Disease Cancer Cardiovascular Disease COVID-19 Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory 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 GERRC (Gene Editing Rat Resource Center) 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

RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:brachial plexus neuropathy
go back to main search page
Accession:DOID:3690 term browser browse the term
Definition:Diseases of the cervical (and first thoracic) roots, nerve trunks, cords, and peripheral nerve components of the BRACHIAL PLEXUS. Clinical manifestations include regional pain, PARESTHESIA; MUSCLE WEAKNESS, and decreased sensation (HYPESTHESIA) in the upper extremity. These disorders may be associated with trauma (including BIRTH INJURIES); THORACIC OUTLET SYNDROME; NEOPLASMS; NEURITIS; RADIOTHERAPY; and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp1351-2)
Synonyms:exact_synonym: Brachial Plexopathy;   Brachial Plexus Disease;   Brachial Plexus Disorder;   Brachial Plexus Disorders;   Brachial Plexus Neuropathies;   Dejerine Klumpke Palsy;   Erb Duchenne Paralysis;   Erb Palsy;   Erb Paralyses;   Erb Paralysis;   Erb's Palsies;   Erb's Palsy;   Erb-Duchenne Paralyses;   Erbs Palsy;   Klumpke Palsy;   Klumpke Paralysis;   Klumpke's Palsy;   Klumpkes Palsy;   Lower Brachial Plexus Neuropathy;   Lower Brachial Plexus Palsy;   Middle Brachial Plexus Neuropathy;   Paralysis of the Lower Brachial Plexus;   Plexopathies, Brachial;   brachial plexus diseases;   upper brachial plexus neuropathy
 primary_id: MESH:D020516
 alt_id: RDO:0001779
 xref: ICD10CM:G54.0;   NCI:C27194
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
 
amyotrophic neuralgia term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Septin9 septin 9 ISO
ISS		 ClinVar Annotator: match by term: Hereditary Neuralgic Amyotrophy (HNA)
ClinVar Annotator: match by term: Hereditary neuralgic amyotrophy
OMIM:162100		 ClinVar
MouseDO		 PMID:16186812 PMID:17546647 PMID:18492087 PMID:19139049 PMID:19204161 PMID:19451530 PMID:20019224 PMID:22981636 PMID:25741868 PMID:26467025 PMID:28492532 NCBI chr10:106,208,308...106,340,747
Ensembl chr10:106,264,434...106,348,490 		JBrowse link
brachial plexus neuritis term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Septin9 septin 9 ISO hereditary neuralgic amyotrophy, OMIM:604061
ClinVar Annotator: match by OMIM:162100
CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Hereditary Neuralgic Amyotrophy (HNA)
ClinVar Annotator: match by term: Hereditary neuralgic amyotrophy		 OMIM
ClinVar
CTD		 PMID:16186812 PMID:17546647 PMID:18492087 PMID:19139049 PMID:19204161 PMID:19451530 PMID:20019224 PMID:22981636 PMID:25741868 PMID:26467025 PMID:28492532, PMID:16186812 RGD:1599349 NCBI chr10:106,208,308...106,340,747
Ensembl chr10:106,264,434...106,348,490 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16091
    disease of anatomical entity 15341
      nervous system disease 10949
        peripheral nervous system disease 2425
          neuropathy 2243
            brachial plexus neuropathy 1
              Brachial Palsy, Familial Congenital 0
              Radiation Induced Brachial Plexopathy 0
              amyotrophic neuralgia 1
              brachial plexus lesion 0
              brachial plexus neuritis + 1
paths to the root