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Ontology Browser

Parent Terms Term With Siblings Child Terms
osteosclerosis +     
axial osteomalacia 
Axial Osteosclerosis 
Camurati-Engelmann disease +   
Cerebellar Hypoplasia with Endosteal Sclerosis  
craniodiaphyseal dysplasia +   
Craniofacial Dysostosis with Diaphyseal Hyperplasia 
craniometaphyseal dysplasia +   
Distal Osteosclerosis 
Dysosteosclerosis +   
Forney Robinson Pascoe Syndrome  
Hyperostosis Cranialis Interna  
Lethal Osteosclerotic Chondrodysplasia, with Intracellular Inclusions 
melorheostosis +   
Mixed Sclerosing Bone Dystrophy 
osteopathia striata with cranial sclerosis  
osteopetrosis +   
Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY).
Osteopoikilosis +   
Osteosclerosis with Ichthyosis and Fractures 
Osteosclerotic Metaphyseal Dysplasia  
Raine Syndrome  
Whyte Murphy Syndrome 
Worth syndrome  

Exact Synonyms: Albers Schoenberg Disease ;   Albers Schonberg Disease ;   Albers Schönberg Disease ;   Congenital Osteopetrosis ;   Marble Bone Disease ;   Marble Bones, Autosomal Dominant ;   Osteopetroses ;   Osteosclerosis Fragilis ;   marble bone ;   osteosclerosis fragilis generalisata
Narrow Synonyms: Albers Schonberg disease, autosomal dominant ;   High Bone Mass
Primary IDs: MESH:D010022
Alternate IDs: RDO:0001226
Xrefs: GARD:4155 ;   ICD10CM:Q78.2 ;   ICD9CM:756.52 ;   NCI:C26840 ;   OMIM:PS259700 ;   OMIM:PS607634 ;   ORDO:667
Definition Sources: "DO", MESH:D010022

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