Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Thoracic spina bifida with hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Hemimyelocele |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
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. |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Meningomyelocele/myelocele |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida of dorsal region (disorder) |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida of cervical region |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida without hydrocephalus |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida with hydrocephalus |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida aperta |
Is a |
True |
Spina bifida |
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. |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Occult spinal dysraphism sequence |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida of lumbar region |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida with hydrocephalus of late onset |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida with stenosis of aqueduct of Sylvius |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida without mention of hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Cervical spina bifida without mention of hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Thoracic spina bifida without mention of hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Lumbar spina bifida without mention of hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Sacral spina bifida without hydrocephalus - open |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida without hydrocephalus - closed |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Fissured spine |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Rachischisis with hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Myelocele with hydrocephalus (disorder) |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Hydromyelocele with hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Fissured spine with hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Closed spina bifida with Arnold-Chiari malformation |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida without hydrocephalus - open |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Unspecified spina bifida with hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida with hydrocephalus, unspecified |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Other specified spina bifida with hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Other spina bifida with hydrocephalus NOS |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida with hydrocephalus NOS |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida without mention of hydrocephalus, site unspecified |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Unspecified spina bifida without mention of hydrocephalus NOS |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Unspecified spina bifida without hydrocephalus - open |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida NOS |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida with hydrocephalus - closed NOS |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida without mention of hydrocephalus, unspecified |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Other specified spina bifida without hydrocephalus |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Spina bifida without mention of hydrocephalus NOS |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Family history: Spina bifida (situation) |
Associated finding |
False |
Spina bifida |
Inferred relationship |
Some |
1 |
A rare disorder that presents as a flat neural placode (at the level of the skin of the back) that is exposed to the environment. The lack of expansion of the subarachnoid space distinguishes this lesion from myelomeningocele. |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Myelocele with hydrocephalus (disorder) |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Known OR suspected fetal spina bifida with myelomeningocele affecting obstetrical care |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
hydromyéloméningocèle |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
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). |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Lumbar myelocystocele |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Cervical spina bifida without hydrocephalus - open |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Thoracic spina bifida without hydrocephalus - open |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Lumbar spina bifida without hydrocephalus - open |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Fetal spina bifida suspected (situation) |
Associated finding |
False |
Spina bifida |
Inferred relationship |
Some |
1 |
Cutaneous lesion resulting from spinal dysraphism (disorder) |
Associated with |
False |
Spina bifida |
Inferred relationship |
Some |
2 |
Port-wine stain associated with spinal dysraphism (disorder) |
Associated with |
True |
Spina bifida |
Inferred relationship |
Some |
3 |
Neurogenic urinary bladder due to spina bifida (disorder) |
Due to |
True |
Spina bifida |
Inferred relationship |
Some |
1 |
Family history: Spina bifida (situation) |
Associated finding |
True |
Spina bifida |
Inferred relationship |
Some |
1 |
Fetal spina bifida suspected (situation) |
Associated finding |
False |
Spina bifida |
Inferred relationship |
Some |
1 |
Family history: Spina bifida (situation) |
Associated finding |
False |
Spina bifida |
Inferred relationship |
Some |
1 |
Spina bifida of sacral region (disorder) |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Pressure injury due to spina bifida (disorder) |
Due to |
True |
Spina bifida |
Inferred relationship |
Some |
1 |
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. |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Dandy-Walker syndrome with spina bifida |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Fetal spina bifida (disorder) |
Is a |
False |
Spina bifida |
Inferred relationship |
Some |
|
Cutaneous lesion resulting from spinal dysraphism (disorder) |
Due to |
True |
Spina bifida |
Inferred relationship |
Some |
2 |
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. |
Is a |
True |
Spina bifida |
Inferred relationship |
Some |
|
Repair of spina bifida |
Has focus |
True |
Spina bifida |
Inferred relationship |
Some |
2 |
Repair of vertebral arch defect in spina bifida |
Has focus |
True |
Spina bifida |
Inferred relationship |
Some |
3 |