Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
A rare, genetic, primary bone dysplasia syndrome characterized by multiple epiphyseal dysplasia, severely delayed ossification (mainly of the epiphyses, pubic symphysis, hands and feet), abnormal modeling of the bones in hands and feet, abnormal pelvis cartilage persistence, and mild growth retardation. Calcium, phosphate and vitamin D serum levels are typically within normal range, while parathyroid hormone serum levels are normal to slightly elevated. Oligodontia has been rarely associated. |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
2 |
A rare syndrome characterized by sparse hair, osteopenia, intellectual disability, minor facial abnormalities, joint laxity and hypotonia. There have been no further descriptions in the literature since 1992. |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
2 |
Osteopenia with high fracture risk (disorder) |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
1 |
Osteopenia following menopause (disorder) |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
1 |
Osteopenia due to disuse (disorder) |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
1 |
Osteopenia caused by drug (disorder) |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
1 |
A rare, genetic, syndromic intellectual disability characterized by global developmental delay, early-onset seizures, cerebellar atrophy, osteopenia, nystagmus and dysmorphic facial features, including bitemporal narrowing, prominent forehead, anteverted nares. Dysarthria, dysmetria, ataxic gait, spasticity and dysmorphic features have also been associated. |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
3 |
Premenopausal idiopathic osteopenia (disorder) |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
1 |
A rare syndromic intellectual disability characterized by intellectual deficit, short stature, obesity, genital abnormalities, and hand and/or toe contractures. The patients also present with generalized osteoporosis and a history of frequent fractures. This syndrome is similar to Prader-Willi syndrome, but the hand contractures and osteoporosis, together with the lack of hypotonia, indicate this is a different entity. |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
5 |
Secondary osteoporotic fracture of lumbar vertebra |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
1 |
Osteoporosis caused by ionizing radiation |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
1 |
Osteoporosis due to and following radiotherapy |
Associated morphology |
True |
Demineralized structure |
Inferred relationship |
Some |
1 |