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Ontology Browser

Parent Terms Term With Siblings Child Terms
spinal disease +     
achondrogenesis type IA  
achondrogenesis type II  
acromesomelic dysplasia, Maroteaux type  
atelosteogenesis +   
autosomal dominant osteopetrosis 2  
Barre-Lieou syndrome 
bone deterioration disease +   
bone structure disease +   
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy  
chronic recurrent multifocal osteomyelitis  
degenerative disc disease +   
high grade glioma +   
Intervertebral Disc Displacement +   
KBG syndrome  
Klippel-Feil syndrome +   
Laplane Fontaine Lagardere Syndrome 
lethal congenital contracture syndrome +   
Microcephaly Cervical Spine Fusion Anomalies 
Ossification of Posterior Longitudinal Ligament +   
ossification of the posterior longitudinal ligament of spine  
Paget's disease of bone +   
Platybasia +  
scoliosis +   
spinal chordoma +   
Spinal Curvatures +   
Spinal Neoplasms 
Spinal Osteochondrosis +   
Spinal Osteophytosis +   
spinal stenosis 
spondylitis +   
spondylocostal dysostosis +   
spondyloepimetaphyseal dysplasia +   
spondylolisthesis +  
spondylolysis +   
spondylosis +   
A degenerative spinal disease that can involve any part of the VERTEBRA, the INTERVERTEBRAL DISK, and the surrounding soft tissue.
X-linked spondyloepiphyseal dysplasia tarda  
 spondylolysis +   

Exact Synonyms: Lumbar spondylosis with myelopathy ;   Lumbarsacral Spondylosis ;   Spondylogenic compression of lumbar spinal cord ;   Spondylogenic compression of thoracic spinal cord ;   Spondylosis Deformans ;   Thoracic or lumbar spondylosis with myelopathy ;   cervical spondylosis ;   lumbosacral spondylosis without myelopathy ;   spondylosis with myelopathy ;   thoracic spondylosis
Primary IDs: MESH:D055009
Alternate IDs: OMIM:184300 ;   RDO:0006609
Xrefs: ICD10CM:M47 ;   ICD10CM:M47.9 ;   ICD9CM:721.9
Definition Sources: "DO" "DO", "DO" "DO", "DO" "DO", "DO" "DO", "DO" "DO", MESH:D055009

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