| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| NPHP3-related Meckel-like syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| SCALP syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Pelizaeus-Merzbacher disease, connatal variant (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Pelizaeus-Merzbacher disease null syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Hypoplasia of optic nerve due to central nervous system malformation |
Due to |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
2 |
| Pelizaeus-Merzbacher disease in female carrier |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Pseudoprogeria syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| TBCK-related intellectual disability syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| RERE-related neurodevelopmental syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Central nervous system malformation in fetus affecting obstetrical care |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| craniorachischisis |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| anomalie congénitale de l'encéphale |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Disorder of neuronal migration and differentiation |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital malformation of the meninges |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Combined malformation of central nervous system and skeletal muscle (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Cockayne syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| hydroméningocèle (trouble) |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Ectopic glial tissue |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Ecchordosis physaliphora |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Amyelencephalus |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital adhesions of cerebral meninges |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital anomaly of spinal cord |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Persistent cerebral embryonic artery |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Cerebral arteriovenous malformation |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Cilioretinal artery (finding) |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Bregeat's syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital cerebral arteriovenous aneurysm |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital anomaly of cerebral artery (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital aneurysm of anterior communicating artery |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Vein of Galen malformation (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital anomaly of organ of Corti |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital anomaly of optic nerve |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| anomalie congénitale de l'encéphale |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Dural arteriovenous malformation |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital arteriovenous fistula of brain |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital aneurysm of anterior communicating artery |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital anomaly of cerebrovascular system |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Fetus with central nervous system malformation |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Amyelencephalus |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Disorder of neuronal migration and differentiation |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Schisis association syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Cerebrooculonasal syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Isotretinoin embryopathy-like syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Cerebral gigantism jaw cysts syndrome (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Congenital absence of optic chiasma (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Ectopic grey matter |
est un(e) (attribut) |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|
| Oro-facial digital syndrome type 12 |
est un(e) (attribut) |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Some |
|