Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital dysarthria |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Combined malformation of central nervous system and skeletal muscle (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital anomaly of nervous system |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital spastic foot |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital athetosis |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
[X]Cerebral palsy and other paralytic syndromes |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Late secondary abnormalities of the central nervous system |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
dysgénésie cérébrale |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
kyste dermoïde de l'encéphale |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Hamartoma of brain |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Aqueduct of Sylvius anomaly |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Rathke's pouch cyst |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital anomaly of nervous system |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Aplasia of corpus callosum |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Immature autonomic system (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Partial absence of septum pellucidum (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Spinal meningocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Cervical spinal hydromeningocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Cystic dermoid choristoma of spinal cord |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Intramedullary glomus arteriovenous malformation of spinal cord (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Intramedullary and extramedullary arteriovenous malformation of spinal cord (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Cerebrovascular system anomalies |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
microcéphalie |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Cavernous hemangioma of brain (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
kyste cérébral congénital |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
hydroméningocèle |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Temporal encephalocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
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 and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Parietal encephalocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Fetus with central nervous system malformation |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Anencephalus |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Hemianencephaly |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital cerebral hernia |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Cerebral arteriovenous malformation |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Spinal hydromeningocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Fetal malformation of central nervous system |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Melanocytoma of meninges |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Melanocytoma of optic nerve head |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital spinal meningocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Olivary heterotopia |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Optic disc dysplasia (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital hypoplasia of brain |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Occipital encephalocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Klippel-Feil sequence |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Cortical dysplasia |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital stricture of cerebral artery |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Developmental displacement of brachial plexus |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital enlargement of ventricle of brain (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital stenosis of aqueduct of Sylvius |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Hypomyelination neuropathy-arthrogryposis syndrome is a rare, genetic, limb malformation syndrome characterized by multiple congenital distal joint contractures (including talipes equinovarus and both proximal and distal interphalangeal joint contractures of the hands) and very severe motor paralysis at birth (i.e. lack of swallowing, autonomous respiratory function and deep tendon reflexes), leading to death within first 3 months of life. Fetal hypo- or akinesia, late-onset polyhydramnios and dramatically reduced, or absent, motor nerve conduction velocities (<10 m/s) are frequently associated. Nerve ultrastructural morphology shows severe abnormalities of the nodes of Ranvier and myelinated axons. |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Cerebrofacial dysplasia |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
diastématomyélie |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Meningoencephalocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Spinal cord hypoplasia |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Ectopic gray matter |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Arachnoid / ependymal cyst |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital abnormal shape of cerebellum |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital hydrocephalus |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Hydromyelia |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital porencephaly |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Megalopapilla (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
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. |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital abnormal shape of cerebrum |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Nasal encephalocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Olive dysplasia |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital cerebral meningocele |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Ectopic pituitary tissue |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Macroencephaly |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Macrogyria |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Atresia of aqueduct of Sylvius |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Accessory pituitary gland |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Occult spinal dysraphism sequence |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Immature ganglionosis of large intestine (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Hypoplasia of the optic nerve |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Foramen of Magendie atresia (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital hypoganglionosis of large intestine (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Congenital coloboma of optic disc |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Foramen of Luschka atresia (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Neuronal choristoma |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Cystic malformation of posterior fossa (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Epileptic encephalopathy with global cerebral demyelination is a rare mitochondrial substrate carrier disorder characterized by severe muscular hypotonia, seizures (with or without episodic apnea) beginning in the first year of life, and arrested psychomotor development (affecting mainly motor skills). Severe spasticity with hyperreflexia has also been reported. Global cerebral hypomyelination is a characteristic imaging feature of this disease. |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Chiari malformation (disorder) |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Cerebellar cortical dysplasia |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Dural arteriovenous malformation |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Myeloschisis |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|
Iniencephaly |
Is a |
False |
Congenital and developmental anomalies of the nervous system |
Inferred relationship |
Some |
|