Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Vascularised bone graft to radius with microsurgery |
Procedure site - Direct (attribute) |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Vascularised bone graft to radius with microsurgery |
Procedure site - Direct (attribute) |
True |
Bone structure of radius |
Inferred relationship |
Some |
3 |
Periosteal suture of radius |
Procedure site - Indirect (attribute) |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Mesomelic dysplasia of upper limb (disorder) |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Brachydactyly-mesomelia-intellectual disability-heart defects syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, intellectual disability, thin habitus with narrow shoulders, mesomelic shortness of the arms, craniofacial dysmorphism (e.g. long lower face, maxillary hypoplasia, beak nose, short columella, prognathia, high arched palate, obtuse mandibular angle), brachydactyly (mostly involving middle phalanges) and cardiovascular anomalies (i.e. aortic root dilatation, mitral valve prolapse). |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
4 |
syndrome de dyschondrostéose - néphropathie |
Finding site |
False |
Bone structure of radius |
Inferred relationship |
Some |
4 |
Mesomelic dysplasia Kantaputra type (MDK) is a rare skeletal disease characterized by symmetric shortening of the middle segments of limbs and short stature. |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
4 |
Mesomelic dysplasia, Savarirayan type is characterized by severely hypoplastic and triangular-shaped tibiae, and absence of the fibulae. So far, two sporadic cases have been described. Moderate mesomelia of the upper limbs, proximal widening of the ulnas, pelvic anomalies and marked bilateral glenoid hypoplasia were also reported. |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Congenital radioulnar synostosis |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Radioulnar synostosis following traumatic injury (disorder) |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Surgical lengthening of radius and ulna with autografts (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of radius |
Inferred relationship |
Some |
4 |
Osteochondroma of radius (disorder) |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Osteomyelitis of radius |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Osteitis deformans of radius and ulna (disorder) |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Plain X-ray of radius and ulna (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Plain X-ray of radius and ulna normal |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
3 |
Plain X-ray of radius normal |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Plain X-ray of radius and ulna abnormal |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
3 |
Plain X-ray of radius abnormal |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Osteoporotic fracture of radius |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome is characterized by the association of proximal fusion of the radius and ulna with congenital amegakaryocytic thrombocytopenia. Less than 10 cases have been reported in the literature so far. The syndrome is transmitted as an autosomal dominant trait and is caused by mutations in the HOXA11 gene (7p15). |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
3 |
Radioulnar synostosis-developmental delay-hypotonia syndrome, also known as Der Kaloustian-McIntosh-Silver syndrome, is an extremely rare syndrome with synostosis described in about 4 patients to date with clinical manifestations including congenital unilateral radioulnar synostosis, generalized hypotonia, developmental delay, and dysmorphic facial features (long face, prominent nose and ears). |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
3 |
Antley-Bixler syndrome |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
5 |
Aneurysmal bone cyst of radius (disorder) |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Osteolysis of radius |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Hypertrophy of radius (disorder) |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Osteonecrosis of radius |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Prophylactic treatment of radius and ulna with methyl methacrylate |
Procedure site - Direct (attribute) |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Disorder of bone and cartilage of radius (disorder) |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
2 |
Aplasia of radius |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Congenital abnormal slender shape of radius (disorder) |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Asymmetric dysplasia of radius |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |
Congenital dysplasia of radius (disorder) |
Finding site |
True |
Bone structure of radius |
Inferred relationship |
Some |
1 |