Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Cleidocranial dysostosis |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital pseudoarthrosis of clavicle (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hypoplasia of clavicle |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Agenesis of clavicle |
Is a |
False |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lack of ossification of clavicle (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital thickening of clavicle |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Crane Heise syndrome (disorder) |
Is a |
False |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Incomplete ossification of clavicle |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cleidorhizomelic syndrome (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital malformation of bone of thorax (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Thoracic myelocystocele |
Is a |
False |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare closed dysraphism with stalk characterized by a dorsal midline dermal sinus tract lined by keratinizing 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 fibers 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 |
Existential restriction modifier (core metadata concept) |
|
Totally absent pericardium |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital cardiospasm (disorder) |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
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 |
Existential restriction modifier (core metadata concept) |
|
Aplasia of clavicle |
Is a |
True |
Congenital anomaly of thorax |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|