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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Adamantinomatous Craniopharyngioma 
Al-Gazali syndrome 
bone disease +   
Diseases of BONES. Diseases of bones.
bone marrow disorder +   
brachydactyly +  
brachydactyly-syndactyly syndrome 
brachydactyly-syndactyly-oligodactyly syndrome 
Brachymorphism-onychodysplasia-dysphalangism syndrome 
Buschke-Ollendorff syndrome 
cartilage disease +   
cartilage-hair hypoplasia +  
cervical spondylosis 
cherubism 
chondroma +  
Coffin-Siris syndrome +  
endocrine-cerebro-osteodysplasia syndrome 
fibrodysplasia ossificans progressiva 
flatfoot  
Hammer Toe Syndrome  
joint disease +   
Marfan syndrome +  
metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria 
microcephaly-brachydactyly-kyphoscoliosis syndrome 
multiple congenital anomalies-hypotonia-seizures syndrome 3 
ossification of the posterior longitudinal ligament of the spine  
Papillary Craniopharyngioma 
polydactyly +  
primary basilar invagination 
Pubic Symphysis Diastasis 
Rare genetic bone development disorder +   
rheumatic disease +   
Rienhoff syndrome 
scalp defects-postaxial polydactyly syndrome 
short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis 
short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome 
symphalangism +  
syndactyly +  
Synovial Chondromatosis 
Teebi-Shaltout syndrome 
temtamy preaxial brachydactyly syndrome 
tooth disease +   
vertebral column disorder +   

Synonyms
Exact Synonyms: DOID:0080001 ;   bone disorder ;   bone element disease ;   bone element disease or disorder ;   disease of bone element ;   disease or disorder of bone element ;   disorder of bone element ;   http://identifiers.org/medgen/14182 ;   http://identifiers.org/mesh/D001847 ;   http://identifiers.org/snomedct/76069003
Related Synonyms: rare bone disease related to a common gene or pathway defect ;   skeletal disease
Xrefs: DOID:0080001 ;   ICD10:M46 ;   ICD10:M48 ;   ICD10:M49 ;   ICD10:M84 ;   ICD10:M89 ;   ICD10:M90 ;   ICD10CM:M80-M85 ;   ICD9:731.8 ;   ICD9:733.99
External Ontologys: disease_has_location EFO:UBERON:0002481 ;   has_disease_location EFO:UBERON:0001474
Definition Sources: MESH:D001847

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