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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 +   
A bone disease that has_material_basis_in an abnormality in the location or function of the skeletal structure. (DO)
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 
spondylitis +   
Spondylocamptodactyly 
spondylocostal dysostosis +   
spondyloepimetaphyseal dysplasia +   
spondylosis +   
 scoliosis +   
 spondylolysis +   
 spondylosis +   

Synonyms
Definition Sources: http://en.wikipedia.org/wiki/Human_skeleton "DO"

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