Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hirschsprung disease, ganglioneuroblastoma syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Mitochondrial DNA depletion syndrome hepatocerebrorenal form |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital muscular dystrophy with intellectual disability and severe epilepsy |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Inherited congenital spastic tetraplegia |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital sacral meningocele |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Severe intellectual disability, progressive spastic diplegia syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Recessive mitochondrial ataxia syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Familial congenital mirror movements |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
PPM-X syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Gillespie syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked acrogigantism due to Xq26 microduplication |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Saldino-Mainzer dysplasia |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital central hypoventilation |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
congenitale uitval van nervus facialis |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Neurocutaneous melanosis |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Combined deficiency of sialidase AND beta galactosidase |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital cataract with ataxia and deafness syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Autosomal recessive Charcot-Marie-Tooth disease type 2 |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Aspartylglucosaminuria |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Hereditary cavernous hemangioma of brain (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Neurocutaneous syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Encephalocraniocutaneous lipomatosis |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Microcephalus, complex motor and sensory axonal neuropathy syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital isolated growth hormone deficiency |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Lipoma due to neurospinal dysraphism |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Fried syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Intellectual disability, spasticity, ectrodactyly syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Acyl-CoA oxidase deficiency |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Macrocephaly with spastic paraplegia and dysmorphism syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Allan-Herndon-Dudley syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Severe X-linked mitochondrial encephalomyopathy (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Spastic paraplegia, nephritis, deafness syndrome (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked neurodegenerative syndrome Bertini type (disorder) |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Progressive congenital rubella encephalitis (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Christianson syndrome |
Is a |
False |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Prenatal-onset spinal muscular atrophy with congenital bone fractures (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital palsy of trochlear nerve (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital oculomotor nerve palsy (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital fibrosis syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital horizontal gaze palsy (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital isolated adrenocorticotropic hormone deficiency (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Maroteaux-Lamy syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Amyotonia congenita |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Schwartz-Jampel syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
GM1 gangliosidosis |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Digital extensor muscle aplasia with polyneuropathy (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Deafness, encephaloneuropathy, obesity, valvulopathy syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Contiguous ABCD1 DXS1357E deletion syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital cataract, hearing loss, severe developmental delay syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Encephalopathy due to prosaposin deficiency (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Ganglioside GM3 synthase deficiency (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Thiamine-responsive encephalopathy (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Sialidosis type 1 (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Mucolipidosis type IV (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Deficiency of alpha-ketoglutarate dehydrogenase (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
3-phosphoglycerate dehydrogenase deficiency juvenile form (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
3-phosphoglycerate dehydrogenase deficiency infantile form (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Lipoic acid synthetase deficiency (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Progressive myoclonic epilepsy type 3 |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital muscular dystrophy with intellectual disability |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Combined oxidative phosphorylation defect type 11 |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Navajo neurohepatopathy |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital myasthenic syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Multiple mitochondrial dysfunctions syndrome type 3 |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Megaconial congenital muscular dystrophy |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital insensitivity to pain with severe intellectual disability (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Albinism with deafness syndrome (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital axonal neuropathy with encephalopathy |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital pseudopapilledema (disorder) |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Oculocerebrodental syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Congenital hydrocephalus caused by toxoplasmosis |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Encephalocele |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|
Dysequilibrium syndrome |
Is a |
True |
Congenital neurological disorder (disorder) |
Inferred relationship |
Some |
|