Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
hydromyéloméningocèle |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
6 |
Rachischisis is a neural tube defect, which occurs when the neural folds do not join at the midline and the undifferentiated neuroectoderm remains exposed. Rachischisis totalis (holorachischisis) is the extreme form in which the entire spinal cord remains open. |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Lumbar spina bifida with hydrocephalus |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Lumbar spina bifida with hydrocephalus - open |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Spina bifida with hydrocephalus - closed |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Spina bifida with hydrocephalus of late onset |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Spina bifida with stenosis of aqueduct of Sylvius |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
A rare closed neural tube defect characterized by cystic dilatation of the central canal of the spinal cord, herniating through a posterior vertebral arch defect (spina bifida) into an expanded cerebrospinal fluid (CSF) filled dural sac (meningocele). It can be located at the caudal part of the spinal cord (terminal myelocystocele) or above conus (non-terminal myelocystocele). |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Cervical myelocystocele |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Thoracic myelocystocele |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Lumbar myelocystocele |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Lumbar spina bifida without hydrocephalus - open |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Sacral spina bifida without hydrocephalus - open |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Spina bifida without hydrocephalus - closed |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Thoracolumbar spina bifida without hydrocephalus - closed |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Fissured spine |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Rachischisis with hydrocephalus |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Myelocele with hydrocephalus (disorder) |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Hydromyelocele with hydrocephalus |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Fissured spine with hydrocephalus |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Closed spina bifida with Arnold-Chiari malformation |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Thoracolumbar spina bifida with hydrocephalus - closed (disorder) |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Hemimyelocele |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
A type of spina bifida aperta that is usually caused by a vertebral defect associated with a superficial fatty mass (lipoma or fatty tumour) that merges with the lower level of the spinal cord. |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Spina bifida with hydrocephalus - open |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Spina bifida without hydrocephalus - open |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Myelomeningocele without hydrocephalus (disorder) |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Lipomyelomeningocele |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Occult spinal dysraphism sequence |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Czeizel-Losonci syndrome (CLS) is an exceedingly rare, severe, congenital genetic malformation disorder characterized by split hand/split foot, hydronephrosis, and spina bifida. Spinal and skeletal manifestations were thoracolumbar scoliosis, spina bifida (spina bifida occulta or spina bifida cystic), Bochdalek diaphragmatic hernia, and radial defects. There have been no further descriptions in the literature since 1987. |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
9 |
Myelomeningocele co-occurrent with hydrocephalus (disorder) |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
8 |
Occult spinal dysraphism sequence |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Primary tethered cord syndrome is a genetic, non-syndromic congenital malformation of the neurenteric canal, spinal cord and column characterized by progressive neurologic deterioration (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal changes (foot deformities and asymmetry, muscle atrophy, limb weakness and numbness, gait disturbances, scoliosis) and/or genitourinary manifestations (bladder and bowel dysfunction). Midline cutaneous stigmata in the lumbosacral region, such as tufts of hair, skin appendages, dimples, subcutaneous lipomas, skin discoloration or hemangiomas, are frequently associated. |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
4 |
Spina bifida of sacral region (disorder) |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Spina bifida of cervical region |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
A type of spina bifida aperta that is usually caused by a vertebral defect associated with a superficial fatty mass (lipoma or fatty tumour) that merges with the lower level of the spinal cord. |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Spina bifida with stenosis of aqueduct of Sylvius |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Spina bifida with hydrocephalus of late onset |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Spina bifida of dorsal region (disorder) |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Myelomeningocele co-occurrent with hydrocephalus (disorder) |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Thoracic spina bifida without hydrocephalus - open |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Thoracic spina bifida with hydrocephalus - open |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Thoracic spina bifida with hydrocephalus |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Lumbar spina bifida without hydrocephalus - closed |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Czeizel-Losonci syndrome (CLS) is an exceedingly rare, severe, congenital genetic malformation disorder characterized by split hand/split foot, hydronephrosis, and spina bifida. Spinal and skeletal manifestations were thoracolumbar scoliosis, spina bifida (spina bifida occulta or spina bifida cystic), Bochdalek diaphragmatic hernia, and radial defects. There have been no further descriptions in the literature since 1987. |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Thoracic spina bifida without hydrocephalus - closed |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Rachischisis with hydrocephalus |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Cervical spina bifida without hydrocephalus - open |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Cervical spina bifida without hydrocephalus - closed |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Spina bifida aperta of cervical spine (disorder) |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
4 |
Spina bifida with hydrocephalus - closed |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Fissured spine with hydrocephalus |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Lumbar spina bifida with hydrocephalus - open |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
5 |
Sacral spina bifida without hydrocephalus - closed |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Dandy-Walker syndrome with spina bifida |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
5 |
hydromyéloméningocèle |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Split spinal cord malformation (disorder) |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Congenital spinal meningocele |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Meningomyelocele of lumbosacral spine (disorder) |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Lipomyelomeningocele |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Congenital spinal hydromeningocele |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
Meningomyelocele (disorder) |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Fetal spina bifida (disorder) |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Faun tail syndrome |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
3 |
hydromyélocèle |
Finding site |
False |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
Structure of fetal arch of vertebra (body structure) |
Is a |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
|
Rachischisis is a neural tube defect, which occurs when the neural folds do not join at the midline and the undifferentiated neuroectoderm remains exposed. Rachischisis totalis (holorachischisis) is the extreme form in which the entire spinal cord remains open. |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
4 |
Rachischisis is a neural tube defect, which occurs when the neural folds do not join at the midline and the undifferentiated neuroectoderm remains exposed. Rachischisis partialis (merorachischisis) is the partial form where the spinal cord is partially closed and partially open. |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
Posterior meningocele is a rare neural tube closure defect characterized by the herniation of a cerebrospinal fluid-filled sac, that is lined by dura and arachnoid mater, through a posterior spina bifida and covered by a layer of skin of variable thickness, which may be dysplastic or ulcerated. The spinal cord and nerves are generally not included and function normally, although sometimes a tethered cord may be associated. They are most commonly located in the lumbar or sacral region. |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
A rare syndromic central nervous system malformation characterized by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11. |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
1 |
A rare, closed spinal dysraphism with characteristics of a myelocystocele at the termination of the spinal cord. It may be an isolated anomaly or be associated with other defects, including sacral agenesis, anorectal and genitourinary anomalies. The conus is not identifiable. The myelocystocele sac may have a significant lipomatous component (terminal lipomyelocystocele). |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |
A rare closed spinal dysraphism with characteristics of myelocystocele located above the conus region. Also considered as a form of saccular limited dorsal myeloschisis. |
Finding site |
True |
Structure of arch of vertebra |
Inferred relationship |
Some |
2 |