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Results 1 - 10 of 506 for bone disease
  1. Osteopetrosis is a bone disease that makes bone tissue abnormally compact and dense and also prone to breakage (fracture). Researchers have described several major ...
  2. ... Familial osteoectasia Hyperostosis corticalis deformans juvenilis Hyperphosphatasemia with bone disease Hyperphosphatasia, familial idiopathic Idiopathic hyperphosphatasia JPD Juvenile Paget' ...
  3. Melorheostosis is a rare bone disease. It causes the abnormal growth of new bone tissue on the surface of existing bones. The new bone has a ... to children. It arises from somatic mutations in bone cells that occur during an individual's ... Candle wax disease Flowing hyperostosis Hyperostosis, monomelic Leri syndrome Leri's ...
  4. ... pass X-linked traits to their sons. Brittle bone disease Fragilitas ossium OI Vrolik disease Genetic Testing Registry: ... Osteogenesis imperfecta, type 19 Dentinogenesis imperfecta ... imperfecta: new genes reveal novel mechanisms in bone dysplasia. Transl Res. 2017 Mar;181:27-48. ...
  5. ... TNFRSF11A gene are responsible for several other rare bone diseases, including two very similar disorders called familial expansile ... in the TNFRSF11A gene can cause several different bone diseases.TNFRSF11A gene mutations also cause a bone disease ...
  6. ... Bone Paget disease Genetic Testing Registry: Hyperphosphatasemia with bone disease Genetic Testing Registry: Paget disease of bone 2, ... Paget disease of bone 6 Paget disease of bone Paget disease of bone, familial Disease InfoSearch National Organization for ...
  7. ... dementia Lower motor neuron degeneration with Paget-like bone disease Multisystem proteinopathy Muscular dystrophy, limb-girdle, with Paget disease of bone Pagetoid amyotrophic lateral sclerosis Pagetoid neuroskeletal syndrome Genetic ...
  8. ... with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance. ...
  9. ... of Gaucher disease may also have eye abnormalities, bone disease, and mild enlargement of the spleen (splenomegaly). Gaucher ...
  10. ... osteolysis, nodulosis, and arthropathy (MONA), a rare inherited bone disease that is characterized by the loss of bone tissue (osteolysis), particularly in the hands and feet, ...
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