Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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:spondylosis
go back to main search page
Accession:DOID:2247 term browser browse the term
Definition:A bone structure disease that involves degeneration between vertebra located_in vertebral column. (DO)
Synonyms:exact_synonym: Spondylosis Deformans;   spondylosis with myelopathy
 narrow_synonym: cervical spondylosis;   lumbar spondylosis with myelopathy;   lumbarsacral spondylosis;   lumbosacral spondylosis without myelopathy;   spondylogenic compression of lumbar spinal cord;   spondylogenic compression of thoracic spinal cord;   thoracic or lumbar spondylosis with myelopathy;   thoracic spondylosis
 primary_id: MESH:D055009
 alt_id: MIM:184300
 xref: EFO:0009610;   ICD10CM:M47;   ICD10CM:M47.9;   ICD9CM:721.9;   MONDO:0002253
For additional species annotation, visit the Alliance of Genome Resources.



show annotations for term's descendants           Sort by:
spondylosis term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Kl Klotho susceptibility ISO RGD PMID:12110410 RGD:10403053 NCBI chr12:490,402...531,417
Ensembl chr12:490,399...530,080
JBrowse link
spondylolysis term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Slc26a2 solute carrier family 26 member 2 ISO DNA:mutations:cds:c.2286A>T(p.D673V), c.1922A>G(p.H641R),g.18654T>C(human) RGD PMID:26077908 RGD:13208868 NCBI chr18:54,648,276...54,666,627
Ensembl chr18:54,652,951...54,666,626
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19100
    disease of anatomical entity 18440
      musculoskeletal system disease 8492
        bone disease 4413
          spinal disease 1147
            spondylosis 2
              spondylolysis + 1
Path 2
Term Annotations click to browse term
  disease 19100
    disease of anatomical entity 18440
      Skin and Connective Tissue Diseases 7809
        connective tissue disease 5960
          bone disease 4413
            spinal disease 1147
              spondylosis 2
                spondylolysis + 1
paths to the root