Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hydromyelia |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Myelodysplasia of spinal cord |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Spinal hamartoma |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neuroenteric cyst and associated malformation |
Is a |
False |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Diplomyelia |
Is a |
False |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Myeloschisis |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Craniorachischisis |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Encephalocele |
Is a |
False |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Spina bifida |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemimyelia |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Amyelia |
Is a |
False |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Exencephaly |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Anencephalus (disorder) |
Is a |
False |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acrania |
Is a |
False |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Faun tail syndrome |
Is a |
False |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
hydromyéloméningocèle |
Is a |
False |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Amniocentesis for possible neural tube defect (procedure) |
Has focus |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Serum neural tube defect screening test |
Has focus |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Split spinal cord malformation (disorder) |
Is a |
False |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cataract, congenital heart disease, neural tube defect syndrome |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Leptomyelolipoma (disorder) |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neurenteric cyst (disorder) |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lipomyelomeningocele (disorder) |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Myelic limited dorsal malformation |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Chaotic conus spinal cord lipoma |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare closed lipomatous, dysraphic malformation of the lower spinal cord characterized by extramedullary lipomatous mass attached to the conus region. The conus is dysplastic and poorly delineated. Various morphological subtypes are recognized. Possible symptoms include bowel and bladder dysfunction and neuro-orthopedic deformity of the lower limbs. |
Is a |
True |
Neural tube defect |
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 |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital retained medullary spinal cord |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital non-dysraphic lipoma of medulla of spinal cord (disorder) |
Is a |
True |
Neural tube defect |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|