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Ontology Browser

Term:
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 structure disease +   
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy  
chronic recurrent multifocal osteomyelitis  
degenerative disc disease +   
hypochondrogenesis  
Intervertebral Disc Displacement +   
KBG syndrome  
Klippel-Feil syndrome +   
Laplane Fontaine Lagardere Syndrome 
lethal congenital contracture syndrome +   
malignant glioma +   
Microcephaly Cervical Spine Fusion Anomalies 
Ossification of Posterior Longitudinal Ligament +   
ossification of the posterior longitudinal ligament of spine  
Paget's disease of bone +   
Platybasia +  
spinal chordoma +   
Spinal Curvatures +   
Spinal Neoplasms 
Spinal Osteochondrosis +   
Spinal Osteophytosis +   
spinal stenosis 
Narrowing of the spinal canal.
spondylitis +   
Spondylocamptodactyly 
spondylocostal dysostosis +   
spondyloepimetaphyseal dysplasia +   
spondylosis +   

Synonyms
Exact Synonyms: Spinal Stenoses ;   Spinal stenosis of lumbar region ;   cervical spinal stenosis ;   lumbar spinal stenosis
Primary IDs: MESH:D013130 ;   RDO:0006602
Xrefs: ICD10CM:M48.0 ;   ICD10CM:M48.00 ;   ICD10CM:M48.02 ;   ICD10CM:M48.06 ;   ICD10CM:M48.061 ;   ICD9CM:723.0 ;   ICD9CM:724.00
Definition Sources: http://en.wikipedia.org/wiki/Spinal_stenosis "DO", http://www.mayoclinic.com/health/spinal-stenosis/DS00515 "DO", http://www.nlm.nih.gov/medlineplus/ency/article/000441.htm "DO", http://www.spinalstenosis.org/ "DO", MESH:D013130

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