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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:amyotrophic neuralgia
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Accession:DOID:10383 term browser browse the term
Synonyms:exact_synonym: Hereditary Neuralgic Amyotrophies;   amyotrophic neuralgias;   hereditary neuralgic amyotrophy;   hereditary neuralgic amyotrophy (HNA);   neuralgic amyotrophies;   neuralgic amyotrophy
 xref: ICD9CM:353.5
For additional species annotation, visit the Alliance of Genome Resources.


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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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16085
    disease of anatomical entity 15340
      nervous system disease 10967
        peripheral nervous system disease 2498
          Neuralgia 47
            amyotrophic neuralgia 1
Path 2
Term Annotations click to browse term
  disease 16085
    disease of anatomical entity 15340
      nervous system disease 10967
        peripheral nervous system disease 2498
          neuropathy 2319
            brachial plexus neuropathy 1
              amyotrophic neuralgia 1
paths to the root