Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital hemiplegia (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Leber's optic atrophy |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Pyridoxine-dependent epilepsy (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Spinal hydromeningocele |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked distal arthrogryposis multiplex congenita (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Microcephaly-capillary malformation syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Odontotrichomelic syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital syphilitic meningitis |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Microphthalmia with brain atrophy syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital sixth nerve palsy (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Microcephalus microcornea syndrome of Seemanova type (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital atrophy of optic nerve (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Malformation of central nervous system of fetus (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Spondyloenchondromatosis with basal ganglia calcification (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
hereditaire nefrogene diabetes insipidus (aandoening) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Cervical hypertrichosis and peripheral neuropathy syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Late congenital neurosyphilis |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Primary congenital glaucoma (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Progressive congenital rubella encephalomyelitis |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Growth delay due to insulin-like growth factor type 1 deficiency (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Hemianencephaly |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Marinesco-Sjögren syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Frontoethmoidal encephalocele |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital cerebral hernia |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital porencephalic cyst (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital quadriplegia |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Ethylmalonic encephalopathy (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital combined disorder of muscle and peripheral nerve (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital nuclear ophthalmoplegia |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital anomaly of nervous system |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital anosmia |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Neu-Laxova syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Acrootoocular syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
FOXG1 syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Ataxia-telangiectasia syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Dementia with Down syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Thyrocerebrorenal syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Menkes kinky-hair syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked distal spinal muscular atrophy type 3 (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked non progressive cerebellar ataxia (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked hereditary motor and sensory neuropathy |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Hypotonia, speech impairment, severe cognitive delay syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked sideroblastic anemia with spinocerebellar ataxia |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Action myoclonus renal failure syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Spastic ataxia with congenital miosis |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-gebonden acromegalie |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Spectrin-associated autosomal recessive cerebellar ataxia |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Familial hyperprolactinemia |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Charcot-Marie-Tooth disease type 4 (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Autosomal dominant intermediate Charcot-Marie-Tooth disease type C (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital meningocele |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Rolandic epilepsy, speech dyspraxia syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Autosomal dominant slowed nerve conduction velocity |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Familial focal epilepsy with variable foci |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Autosomal dominant congenital benign spinal muscular atrophy |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
HIVEP2-related intellectual disability |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital trigeminal anesthesia (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
5q31.3 microdeletion syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Myosclerosis (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
hydromeningocele |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Multiple congenital anomalies, hypotonia, seizures syndrome type 2 |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Pitt-Hopkins-achtig syndroom (aandoening) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Late congenital syphilitic polyneuropathy (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Infantile spasm and broad thumb syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital Horner syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Jawad syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Ptosis and vocal cord paralysis syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Aganglionosis of large intestine (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Familial congenital palsy of trochlear nerve (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Hirschsprung disease, ganglioneuroblastoma syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|