Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Percutaneous microwave ablation of neoplasm of bone using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
2 |
Percutaneous cryoablation of neoplasm of bone using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
1 |
Percutaneous cryoablation of neoplasm of bone using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
2 |
CT guided percutaneous cryoablation of neoplasm of bone |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
1 |
CT guided percutaneous cryoablation of neoplasm of bone |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
2 |
Percutaneous cryoablation of neoplasm of bone using fluoroscopic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
1 |
Percutaneous cryoablation of neoplasm of bone using fluoroscopic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
2 |
CT guided percutaneous microwave ablation of neoplasm of bone |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
1 |
CT guided percutaneous microwave ablation of neoplasm of bone |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
2 |
Percutaneous microwave ablation of neoplasm of bone using fluoroscopic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
1 |
Percutaneous microwave ablation of neoplasm of bone using fluoroscopic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
2 |
Percutaneous laser ablation of neoplasm of bone using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
1 |
Percutaneous laser ablation of neoplasm of bone using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
2 |
Open reduction of fracture and internal fixation with tension band wiring (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
1 |
Open reduction of fracture and internal fixation with tension band wiring (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
2 |
A rare skeletal dysplasia characterized by disproportionate short stature with short limbs, small hands and feet, and midface hypoplasia with small nose. Mild spondylar dysplasia, delayed epiphyseal ossification of the hip and knee, and severe brachydactyly with cone shaped phalangeal epiphyses are characteristic features. In adulthood, premature spondylosis and degenerative joint disease develop in some patients. Frequent respiratory infections with prolonged cough and inspiratory stridor, consistent with laryngomalacia, can also be present. Intelligence, dentition, hearing and visual acuity are not affected. |
Finding site |
True |
Bone structure |
Inferred relationship |
Some |
1 |
A rare primary bone dysplasia with increased bone density characterized by lethal neonatal dwarfism with hydrops. Cortical thickening throughout the skeleton, particularly in the long bones and ribs, brachycephaly, severe brachydactyly and craniofacial abnormalities are reported. |
Finding site |
True |
Bone structure |
Inferred relationship |
Some |
1 |
Dysplastic cortical hyperostosis Kozlowski Tsuruta type is a form of rare dysplastic cortical hyperostosis characterized by narrow chest, short limbs with generalized, symmetrical cortical thickening throughout the skeleton, particularly in the long bones and ribs. Additional features may include sclerotic metacarpals and metatarsals with proximal tapering and mild sclerosis of the pelvis. No cortical thickening was reported in skull or mandible. Size of the hands and feet are normal. Microcephaly, abnormal lung segmentation, hepatosplenomegaly, poorly developed cerebral sulci and complete renal duplication has been observed. It is a lethal condition associated to severe fetal hydrops and polyhydramnios. |
Finding site |
True |
Bone structure |
Inferred relationship |
Some |
1 |
Dysplastic cortical hyperostosis Al-Gazali type is a form of rare dysplastic cortical hyperostosis characterized by narrow chest, short limbs with generalized, symmetrical cortical thickening throughout the skeleton, particularly in the long bones and ribs. Additional features may include sclerotic metacarpals and metatarsals with proximal tapering and mild sclerosis of the pelvis. No cortical thickening reported in skull or mandible. Size of the hands and feet are normal. Microcephaly, abnormal lung segmentation, hepatosplenomegaly, poorly developed cerebral sulci and complete renal duplication has been observed. It is a lethal condition associated to severe fetal hydrops and polyhydramnios. |
Finding site |
True |
Bone structure |
Inferred relationship |
Some |
1 |
Percutaneous fixation using Kirschner wire |
Procedure site - Direct (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
1 |
A rare type of Ehlers-Danlos syndrome characterised by connective tissue defects (joint laxity of finger joints and knees, small joint hypermotility and tissue fragility), vascular complications (atrioventricular defect, symptomatic cerebral aneurysm, vascular dissection) and frontoparietally accentuated polymicrogyria of the cobblestone variant. Specific brain anomalies (including cerebrocortical dysplasia, cerebellar microcysts and white matter anomalies) are present in all patients. Most of the affected individuals have developmental delay and may develop epilepsy. Additional clinical features include spontaneous intracranial hypotension, idiopathic intracranial hypertension, headache, chronic pain syndrome, peripheral neuropathy, plexopathy, translucent skin and clubfoot. Dysmorphic features such as eye anomalies (strabismus, bilateral hyperopia, esotropia, proptosis), pinched nose, thin upper lip, crowded teeth and retrognathia are also reported. |
Finding site |
True |
Bone structure |
Inferred relationship |
Some |
3 |
Removal of external fixation ring from bone |
Procedure site - Indirect (attribute) |
True |
Bone structure |
Inferred relationship |
Some |
1 |