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Ontology Browser

Parent Terms Term With Siblings Child Terms
osteosclerosis +     
ainhum +  
Alpha-2-Deficient Collagen Disease 
Anetoderma +   
arterial tortuosity syndrome  
Au-Kline Syndrome  
axial osteomalacia 
Axial Osteosclerosis 
bone disease +   
Bone Fragility with Contractures, Arterial Rupture, and Deafness  
Camurati-Engelmann disease +   
cartilage disease +   
cellulitis +   
Cerebellar Hypoplasia with Endosteal Sclerosis  
chronic interstitial cystitis 
collagen disease +   
Congenital Fascial Dystrophy 
Connective Tissue Neoplasms +   
craniodiaphyseal dysplasia +   
Craniofacial Dysostosis with Diaphyseal Hyperplasia 
craniometaphyseal dysplasia +   
cutaneous lupus erythematosus +   
cutis laxa +   
dental pulp disease +   
dermatomyositis +   
Distal Osteosclerosis 
Dupuytren Contracture +  
Dysosteosclerosis +   
enthesopathy +  
fasciitis +  
fibrodysplasia ossificans progressiva  
Forney Robinson Pascoe Syndrome  
homocystinuria +   
Hyperostosis Cranialis Interna  
interstitial keratitis +  
interstitial lung disease +   
Lethal Osteosclerotic Chondrodysplasia, with Intracellular Inclusions 
lipodystrophy +   
Marden-Walker Syndrome  
mediastinitis +  
melorheostosis +   
mixed connective tissue disease  
Mixed Sclerosing Bone Dystrophy 
mucinoses +   
Noonan syndrome +   
ochronosis +  
ossification of the posterior longitudinal ligament of spine  
osteopathia striata with cranial sclerosis  
osteopetrosis +   
Osteopoikilosis +   
An asymptomatic, autosomal dominant trait in which pea-sized sclerotic spots, prominent in the metaphyseal area, are accompanied by unique cutaneous lesions. These are yellowish papules or plaques with increased elastin content. (From Cecil Textbook of Medicine, 19th ed, pp1434-35)
Osteosclerosis with Ichthyosis and Fractures 
Peyronie's disease  
plantar fascial fibromatosis 
pseudoxanthoma elasticum +   
Raine Syndrome  
rheumatic disease +   
Stickler syndrome +   
synovitis +   
systemic scleroderma +   
Volkmann contracture 
Whyte Murphy Syndrome 

Exact Synonyms: Osteopoikiloses
Primary IDs: MESH:D010023 ;   RDO:0001479
Xrefs: GARD:4158 ;   NCI:C84985
Definition Sources: MESH:D010023,

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