Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Ectopic neuronal tissue |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Central nervous system malformation in fetus affecting obstetrical care |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Craniorachischisis |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital anomaly of brain |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Amyelencephalus |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital anomaly of spinal cord |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital anomaly of optic nerve |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Disorder of neuronal migration and differentiation |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital malformation of the meninges |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Combined malformation of central nervous system and skeletal muscle |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cockayne syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hydromeningocele |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Ectopic glial tissue |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Ecchordosis physaliphora |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital adhesions of cerebral meninges |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Persistent cerebral embryonic artery |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cerebral arteriovenous malformation |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cilioretinal artery |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Bregeat's syndrome |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital cerebral arteriovenous aneurysm |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital anomaly of cerebral artery |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital aneurysm of anterior communicating artery |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Vein of Galen malformation |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital anomaly of organ of Corti |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital anomaly of brain |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Dural arteriovenous malformation |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital arteriovenous fistula of brain |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital aneurysm of anterior communicating artery |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital anomaly of cerebrovascular system |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Fetus with central nervous system malformation |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Amyelencephalus |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Disorder of neuronal migration and differentiation |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Schisis association syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cerebrooculonasal syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Isotretinoin embryopathy-like syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cerebral gigantism jaw cysts syndrome |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital absence of optic chiasma |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Oro-facial digital syndrome type 12 |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Nephrocystin 3-related Meckel-like syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome |
Is a |
False |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Pelizaeus-Merzbacher disease, connatal variant |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Pelizaeus-Merzbacher disease null syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hypoplasia of optic nerve due to central nervous system malformation |
Due to |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
2 |
Pelizaeus-Merzbacher disease in female carrier |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Pseudoprogeria syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
TBC1 domain containing kinase-related intellectual disability syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|
Myelinated nerve fiber layer of retina |
Is a |
True |
Congenital anomaly of central nervous system |
Inferred relationship |
Existential restriction modifier |
|