| Term Name: | Paget's disease of bone 5 |
|---|---|
| Synonyms: | Familial osteoectasia, Hereditary hyperphosphatasia, Hyperostosis corticalis deformans juvenilis, Juvenile Paget disease, Paget disease of bone-5 |
| Definition: | A Paget's disease of bone that is characterized by short stature, progressive long bone deformities, fractures, vertebral collapse, skull enlargement, and hyperostosis with progressive deafness and that has_material_basis_in osteoprotegerin deficiency caused by homozygous or compound heterozygous mutation in the TNFRSF11B gene on chromosome 8q24. |
| Ontology: | Human Disease [DOID:0081368] ( DOID:0081368 ) |