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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
osteochondrosis +     
spinal disease +     
achondrogenesis type IA  
acromesomelic dysplasia, Maroteaux type  
atelosteogenesis +   
autosomal dominant osteopetrosis 2  
Blount's disease 
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy  
chronic recurrent multifocal osteomyelitis +   
dropped head syndrome 
high grade glioma +   
Intervertebral Disc Displacement +   
KBG syndrome  
Klippel-Feil syndrome +   
Kohler's disease 
Laplane Fontaine Lagardere Syndrome 
Legg-Calve-Perthes disease +   
lethal congenital contracture syndrome +   
Microcephaly with Cervical Spine Fusion Anomalies 
Osgood-Schlatter's disease 
Ossification of Posterior Longitudinal Ligament +   
Osteochondritis +   
Platybasia +  
spinal chordoma +   
Spinal Curvatures +   
Spinal Neoplasms 
Spinal Osteochondrosis +   
A bone disorder involving ossification centers (EPIPHYSES) of the VERTEBRAL COLUMN.
Spinal Osteophytosis +   
spondylitis +   
Spondylocamptodactyly 
spondylocostal dysostosis +   
spondyloepimetaphyseal dysplasia +   
spondylosis +   
Thiemann Disease 
vertebral hypersegmentation and orofacial anomalies  
X-linked spondyloepiphyseal dysplasia tarda  

Synonyms
Exact Synonyms: Osteochondrosis of Spine ;   Spinal Osteochondroses ;   Spine Osteochondroses ;   Spine Osteochondrosis
Primary IDs: MESH:D055035
Xrefs: EFO:0008576
Definition Sources: MESH:D055035

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