Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hydromyelia |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Defective development of cauda equina |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Arnold-Chiari syndrome |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Myelatelia |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spina bifida of dorsal region (disorder) |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
hydromyélocèle |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Congenital anomaly of spinal meninges |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
diastématomyélie |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spina bifida with hydrocephalus |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spinal cord dysplasia |
Is a |
True |
Congenital anomaly of spinal cord |
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 |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Hemimyelia |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spina bifida of lumbar region |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Amyelia |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
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 |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
[X]Other specified congenital malformations of spinal cord |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Congenital syringomyelia (disorder) |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spina bifida of cervical region |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spina bifida of lumbar region |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
hydromyéloméningocèle |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Abnormality of canalization and retrogressive differentiation (disorder) |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
dysgénésie de la queue de cheval |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Diplomyelia |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Myeloschisis |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spina bifida aperta |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
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 |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spinal cord hypoplasia |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
syringomyélobulbie |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spinal hydromeningocele |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Split spinal cord malformation (disorder) |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spina bifida aperta of thoracic spine (disorder) |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spina bifida aperta of cervical spine (disorder) |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
A rare hereditary ataxia characterized by unusual facies (i.e. gross, rough and abundant hair, mild palpebral ptosis, thick lips, and down-curved corners of the mouth), dysarthria, delayed psychomotor development, scoliosis, foot deformities, and ataxia. There have been no further descriptions in the literature since 1985. |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Spina bifida aperta of lumbar spine (disorder) |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Myelomeningocele co-occurrent with hydrocephalus (disorder) |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Intramedullary glomus arteriovenous malformation of spinal cord (disorder) |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Intramedullary and extramedullary arteriovenous malformation of spinal cord (disorder) |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Myelocele with hydrocephalus (disorder) |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Cervical myelocele |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Lumbar myelocele |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Myelodysplasia of spinal cord |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Encephalomyelocele |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Thoracic myelocele |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Familial spinal neurofibromatosis |
Is a |
False |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Lipoma due to neurospinal dysraphism |
Is a |
False |
Congenital anomaly of spinal cord |
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 |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Holoprosencephaly-caudal dysgenesis syndrome is a central nervous system malformation syndrome characterized by holoprosencephaly with microcephaly, abnormal eye morphology (hypotelorism, cyclopia, exophthalmos), nasal anomalies (single nostril or absent nose), and cleft lip/palate, combined with signs of caudal regression (sacral agenesis, sirenomelia with absent external genitalia). |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome is a rare, genetic, neural tube defect malformation syndrome characterized by sacral agenesis and abnormal vertebral body ossification with normal vertebral arches associated with notochord canal persistence on ultrasonography. Additional findings include bilateral clubfoot, oligohydramnios, single umbilical artery and, in some, increased nuchal translucency. |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
A rare dysraphic spinal cord lipoma with characteristics of a lipomatous mass extending ventrally to the dorsal root entry zone, indicating a more severe malformation of the spinal cord. The diagnosis can be suggested on imaging but usually confirmed during surgery. |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
A rare closed dysraphism with terminal stalk with characteristics of persistant rudimentary spinal cord below conus. It contains non-functional neural tissue and is typically isolated. The diagnostic is suggested by attenuated conus without fat, further confirmed by pathological analysis (glioneuronal core with ependyma-lined lumen, nerve roots, and dorsal root ganglia). Differential diagnostic with intraoperative neurophysiological monitoring is mandatory as neuroimaging fails to distinguish it from functional conus. |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
A very rare non-dysraphic spinal cord lipoma which is located within the spinal cord. There is no defect in the overlying dura. |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Aplasia of spinal cord white matter column (disorder) |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|
Neurenteric cyst of spine (disorder) |
Is a |
True |
Congenital anomaly of spinal cord |
Inferred relationship |
Some |
|