Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Short rib-polydactyly syndrome, non-Majewski type |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
6 |
Congenital pectus carinatum |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Congenital pectus excavatum (disorder) |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Open fracture of eight OR more ribs |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Open multiple fractures of lower limb with ribs AND sternum |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
4 |
Multiple fractures of upper limb with sternum AND ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Open fracture of five ribs |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Congenital bent rib |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Congenital misalignment of rib |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Congenital malposition of rib |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Pathological fracture of rib |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Open bilateral fracture of multiple ribs (disorder) |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Grafting of bone of rib (procedure) |
Procedure site - Indirect (attribute) |
False |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Cough fracture of ribs |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Multiple fractures of upper limb with sternum AND ribs |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Congenital focal enlargement of rib |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Congenital fusion of ribs |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Adjustment of vertical expanding prosthetic titanium rib (procedure) |
Procedure site - Indirect (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Biopsy of bone structure of rib using fluoroscopic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Biopsy of bone structure of rib using fluoroscopic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Closed fracture of two ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Closed fracture of five ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Closed fracture of seven ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Open multiple fractures of upper limb with ribs |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
4 |
Open multiple fractures of upper limb with sternum AND ribs |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
4 |
Closed fracture of three ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Closed fracture of six ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Multiple fractures of lower limb with ribs AND sternum |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Closed fracture of eight OR more ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Short rib dysplasia |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Multiple fractures of upper limb with ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Open bilateral fracture of multiple ribs (disorder) |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Closed multiple fractures of lower limb with ribs AND sternum |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
4 |
CT guided biopsy of rib |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
CT guided biopsy of rib |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
X-ray of rib |
Procedure site - Direct (attribute) |
False |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Computed tomography of rib (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
A very rare and mild form of spondylocostal dysostosis characterized by vertebral and costal segmentation defects, often with a reduction in the number of ribs. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Open reduction of fracture of multiple ribs with internal fixation (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Open reduction of fracture of multiple ribs with internal fixation (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Depressed rib (finding) |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Somatic dysfunction of rib (finding) |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Abnormal prominence of rib (finding) |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Cerebro-facio-thoracic dysplasia or Pascual-Castroviejo syndrome type 1 is a rare syndrome characterized by facial dysmorphism, intellectual deficit and costovertebral abnormalities. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Cerebro-facio-thoracic dysplasia or Pascual-Castroviejo syndrome type 1 is a rare syndrome characterized by facial dysmorphism, intellectual deficit and costovertebral abnormalities. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
4 |
Internal fixation of rib (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Thoracolaryngopelvic dysplasia is a short-rib dysplasia characterized by thoracic dystrophy, laryngeal stenosis and a small pelvis. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
7 |
Primary chondrosarcoma of bone of rib (disorder) |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Primary Ewing sarcoma of bone of rib (disorder) |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Bone structure of right rib (body structure) |
Is a |
True |
Bone structure of rib |
Inferred relationship |
Some |
|
Bone structure of left rib (body structure) |
Is a |
True |
Bone structure of rib |
Inferred relationship |
Some |
|
A rare ciliopathy with major skeletal involvement characterized by short ribs with an extremely narrow thorax, very short limbs, absent or very small fibulae, severe metaphyseal dysplasia of tubular bones, post-axial polydactyly, and defective ossification in the calvaria, vertebrae, pelvis, and bones of the hands and feet. Congenital anomalies of multiple other organs have also been described, such as polycystic kidneys, transposition of the great vessels, and atretic lesions of the gastrointestinal and genitourinary tract. Hydrops fetalis may be observed at an early gestational age. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
7 |
Benign osteogenic neoplasm of bone of rib (disorder) |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Dysmorphism-pectus carinatum-joint laxity syndrome is characterised by joint laxity, pectus carinatum and facial dysmorphism (mild frontal bossing, a beaked nose with a low nasal bridge, malar hypoplasia, chubby cheeks, a striking philtrum and arched upper lips). It has been described in two siblings. The mode of transmission is unknown. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
6 |
Jeune syndrome, also called asphyxiating thoracic dystrophy, is a short-rib dysplasia characterized by a narrow thorax, short limbs and radiological skeletal abnormalities including trident aspect of the acetabula and metaphyseal changes. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
A rare genetic developmental defect during embryogenesis characterized by the association of the classic features of Joubert syndrome (congenital midbrain-hindbrain malformations causing hypotonia, abnormal breathing and eye movements, ataxia and cognitive impairment) together with the skeletal anomalies of Jeune asphyxiating thoracic dystrophy (short ribs, long and narrow thorax causing respiratory failure, short-limbs, short stature, and polydactyly). Additional variable manifestations include cystic kidneys, liver fibrosis, and retinal dystrophy. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
5 |
Pectus excavatum-macrocephaly-dysplastic nails syndrome is a rare multiple congenital anomalies syndrome characterized by relative macrocephaly, pectus excavatum, short stature, nail dysplasia, and motor developmental delay (that resolves during childhood). There have been no further descriptions in the literature since 1992. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Acquired pectus excavatum (disorder) |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Imperforate oropharynx-costovertebral anomalies syndrome is a dysostosis with predominant vertebral and costal involvement characterized by oropharyngeal atresia, mild mandibulofacial dysostosis, auricular malformations, and costovertebral anomalies (hemivertebrae, block vertebra, partial fusion of the ribs, absent ribs). There have been no further descriptions in the literature since 1989. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Imperforate oropharynx-costovertebral anomalies syndrome is a dysostosis with predominant vertebral and costal involvement characterized by oropharyngeal atresia, mild mandibulofacial dysostosis, auricular malformations, and costovertebral anomalies (hemivertebrae, block vertebra, partial fusion of the ribs, absent ribs). There have been no further descriptions in the literature since 1989. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
A very rare and mild form of spondylocostal dysostosis characterized by vertebral and costal segmentation defects, often with a reduction in the number of ribs. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Congenital pectus carinatum |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Short rib-polydactyly syndrome, Majewski type |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Cerebro-costo-mandibular syndrome |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Thoracolaryngopelvic dysplasia is a short-rib dysplasia characterized by thoracic dystrophy, laryngeal stenosis and a small pelvis. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Dysmorphism-pectus carinatum-joint laxity syndrome is characterised by joint laxity, pectus carinatum and facial dysmorphism (mild frontal bossing, a beaked nose with a low nasal bridge, malar hypoplasia, chubby cheeks, a striking philtrum and arched upper lips). It has been described in two siblings. The mode of transmission is unknown. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
A rare genetic developmental defect during embryogenesis characterized by the association of the classic features of Joubert syndrome (congenital midbrain-hindbrain malformations causing hypotonia, abnormal breathing and eye movements, ataxia and cognitive impairment) together with the skeletal anomalies of Jeune asphyxiating thoracic dystrophy (short ribs, long and narrow thorax causing respiratory failure, short-limbs, short stature, and polydactyly). Additional variable manifestations include cystic kidneys, liver fibrosis, and retinal dystrophy. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
A rare ciliopathy with major skeletal involvement characterized by short ribs with an extremely narrow thorax, very short limbs, absent or very small fibulae, severe metaphyseal dysplasia of tubular bones, post-axial polydactyly, and defective ossification in the calvaria, vertebrae, pelvis, and bones of the hands and feet. Congenital anomalies of multiple other organs have also been described, such as polycystic kidneys, transposition of the great vessels, and atretic lesions of the gastrointestinal and genitourinary tract. Hydrops fetalis may be observed at an early gestational age. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
4 |
Local excision of lesion of bone of rib |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Schwere früh-beginnende Adipositas mit Insulin-Resistenz-Syndrom durch SH2B1-Mangel |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Closed multiple fractures of upper limb with ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
An extremely rare, lethal, primary bone dysplasia characterized by thin ribs, thin long bones, high-arched palate and facial features of frontal bossing and low-set, posteriorly rotated ears. Bilateral cryptorchidism may be also observed. There have been no further descriptions in the literature since 1990. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
A rare syndromic primary bone dysplasia characterized by short ribs with a narrow chest and thoracic dysplasia, mild rhizomelic shortening of the limbs, communicating hydrocephalus, and developmental delay. There have been no further descriptions in the literature since 1987. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
A rare primary bone dysplasia disorder characterized by a bell-shaped thorax, disproportionate short stature, pelvic hypoplasia, dislocatable radial heads and elongated distal fibulae. No acetabular spurs nor phalangeal cone-shaped epiphyses are present, and osseous manifestations tend to normalize with age. There have been no further descriptions in the literature since 1988. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Schwere früh-beginnende Adipositas mit Insulin-Resistenz-Syndrom durch SH2B1-Mangel |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
1 |
A rare, genetic, congenital limb malformation syndrome characterized by bilateral short broad thumbs, short deviated index fingers, clinodactyly of the fifth fingers, broad, valgus-deviated halluces and laterally-deviated, overlapping second toe, associated with severe pectus excavatum and craniofacial dysmorphism (including brachycephaly, low anterior hairline, flat supraorbital ridges, telecanthus, upslanting palpebral fissures, maxillary hypoplasia, posteriorly rotated ears, microsomia and micrognathia). Radiological findings include thumb, index, and middle finger hyperphalangy, with severe delta phalanxes in affected fingers and halluces. |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
2 |
A rare syndromic craniosynostosis characterized by prenatal presentation with cloverleaf skull, micromelia and asphyxiating thoracic dysplasia. Radiologic features include short ribs, horizontal roof of the acetabulum with a rounded median prominence and lateral spurs, deformed long bones with broad metaphyses, and absent ossification of the terminal phalanges. There have been no further descriptions in the literature since 1987. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Jarcho-Levin syndrome |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Open multiple fractures of upper limb with sternum AND ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
6 |
Short rib polydactyly syndrome |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Type IV short rib polydactyly syndrome |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
A rare ciliopathy with major skeletal involvement characterized by short ribs with an extremely narrow thorax, very short limbs, absent or very small fibulae, severe metaphyseal dysplasia of tubular bones, post-axial polydactyly, and defective ossification in the calvaria, vertebrae, pelvis, and bones of the hands and feet. Congenital anomalies of multiple other organs have also been described, such as polycystic kidneys, transposition of the great vessels, and atretic lesions of the gastrointestinal and genitourinary tract. Hydrops fetalis may be observed at an early gestational age. |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Type III short rib polydactyly syndrome |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Closed multiple fractures of lower limb with ribs AND sternum |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Multiple fractures of lower limb AND ribs |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Flail chest |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Open flail chest |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Open multiple fractures of lower limb with ribs AND sternum |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Closed flail chest |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
4 |
Chondrosarcoma of rib |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Osteosarcoma of bone of rib |
Finding site |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Primary chondrosarcoma of bone of rib (disorder) |
Finding site |
False |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Bone graft of rib with microvascular anastomosis |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Bone graft of rib with microvascular anastomosis |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
3 |
Grafting of bone of rib (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Grafting of bone of rib (procedure) |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
2 |
Bone structure of thirteenth rib (body structure) |
Is a |
True |
Bone structure of rib |
Inferred relationship |
Some |
|
En bloc excision of neoplasm of rib |
Procedure site - Direct (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |
Suture of periosteum of rib |
Procedure site - Indirect (attribute) |
True |
Bone structure of rib |
Inferred relationship |
Some |
1 |