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RGD uses the Human Disease Ontology (DO, 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 neuritis
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Accession:DOID:3689 term browser browse the term
Definition:A syndrome associated with inflammation of the BRACHIAL PLEXUS. Clinical features include severe pain in the shoulder region which may be accompanied by MUSCLE WEAKNESS and loss of sensation in the upper extremity. This condition may be associated with VIRUS DISEASES; IMMUNIZATION; SURGERY; heroin use (see HEROIN DEPENDENCE); and other conditions. The term brachial neuralgia generally refers to pain associated with brachial plexus injury. (From Adams et al., Principles of Neurology, 6th ed, pp1355-6)
Synonyms:exact_synonym: Amyotrophic Neuralgia;   Amyotrophy, Hereditary Neuralgic, with Predilection for Brachial Plexus;   Brachial Neuralgia;   Brachial Neuritides;   Brachial Neuritis;   Brachial Plexus Neuritides;   Cervico Brachial Neuralgia;   Cervico-Brachial Neuralgias;   Cervicobrachial Neuralgia;   Cervicobrachial Neuralgias;   Familial Brachial Plexus Neuritis;   HEREDITARY NEURALGIC AMYOTROPHY (HNA);   HNA;   Hereditary Brachial Plexus Neuropathy;   Hereditary Neuralgic Amyotrophies;   Hereditary Neuralgic Amyotrophy;   Heredofamilial Neuritis with Brachial Plexus Predilection;   NAPB;   Neuritis With Brachial Predilection;   Parsonage Aldren Turner Syndrome;   Parsonage Turner Syndrome;   amyotrophic neuralgias;   brachial neuralgias;   shoulder girdle neuropathies;   shoulder girdle neuropathy
 primary_id: MESH:D020968
 alt_id: OMIM:162100
 xref: ICD10CM:G54.5;   NCI:C84600
For additional species annotation, visit the Alliance of Genome Resources.

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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
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
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16058
    syndrome 6996
      brachial plexus neuritis 1
        Acute Brachial Neuritis 0
Path 2
Term Annotations click to browse term
  disease 16058
    disease of anatomical entity 15305
      nervous system disease 10879
        peripheral nervous system disease 2475
          neuropathy 2296
            neuritis 192
              brachial plexus neuritis 1
                Acute Brachial Neuritis 0
paths to the root


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