Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Cleidocranial dysostosis |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital pseudoarthrosis of clavicle (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital hypoplasia of clavicle |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Agenesis of clavicle |
Is a |
False |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Lack of ossification of clavicle |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital thickening of clavicle |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Crane-Heise syndrome is a very rare syndrome characterized by poorly mineralized calvarium, facial dysmorphism, vertebral abnormalities and absent clavicles. |
Is a |
False |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Incomplete ossification of clavicle |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Cleidorhizomelic syndrome is a rhizo-mesomelic dysplasia characterized by rhizomelic short stature/dwarfism in combination with lateral clavicular defects. Additional manifestations include brachydactyly with bilateral clinodactyly and hypoplastic middle phalanx of the fifth digit. X-ray demonstrated an apparent Y-shaped or bifid distal clavicle. Cleidorhizomelic syndrome has been reported in one family (mother and son) and is suspected to be transmitted in an autosomal dominant manner. There have been no further descriptions in the literature since 1988. |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital malformation of bone of thorax (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Thoracic myelocystocele |
Is a |
False |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
A rare closed dysraphism with stalk characterised by a dorsal midline dermal sinus tract lined by keratinising stratified squamous epithelium extending to the intrathecal space. Other components such as hair follicles and shafts, mesenchymal derivatives (blood vessels and fibrous tissue) and occasionally nerve fibres can be observed. Inflamed granulation tissue containing mixed neutrophils, plasma cells, lymphocytes, and histiocytes is consistently found in the tract. It can also be associated with an intradural dermoid cyst. This malformation is at risk to cause intrathecal infections (meningitis, empyema) that justify prophylactic surgery. |
Is a |
False |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Totally absent pericardium |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital cardiospasm |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect, aortic coarctation, eye abnormality, sternal anomalies syndrome (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Aplasia of clavicle |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital hypoplasia of left side of chest (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital hypoplasia of pectoral muscle (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital hypoplasia of serratus anterior muscle (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital hypoplasia of right side of chest (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|
Congenital dysplasia of thorax (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Some |
|