| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Jawad syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Solute carrier family 35 member A2 congenital disorder of glycosylation |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Optic nerve oedema, splenomegaly syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive leukoencephalopathy, ischaemic stroke, retinitis pigmentosa syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Warburg micro syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Zechi Ceide syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive frontotemporal pachygyria |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Severe neurodegenerative syndrome with lipodystrophy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Childhood-onset spasticity with hyperglycinaemia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Lethal occipital encephalocele, skeletal dysplasia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Deficiency in anterior pituitary function, variable immunodeficiency syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Childhood encephalopathy due to thiamine pyrophosphokinase deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Chudley McCullough syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Porencephaly, microcephaly, bilateral congenital cataract syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Pitt Hopkins-like syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| NPHP3-related Meckel-like syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Multiple congenital anomalies, hypotonia, seizures syndrome type 2 |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| PRKAR1B-related neurodegenerative dementia with intermediate filaments |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial infantile gigantism |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked acrogigantism |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Ferro-cerebro-cutaneous syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Fatal post-viral neurodegenerative disorder |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypomyelination with brain stem and spinal cord involvement and leg spasticity |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Congenital pontocerebellar hypoplasia type 9 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal dominant primary microcephaly |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked acrogigantism |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| FAST kinase domains 2-related infantile mitochondrial encephalomyopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Primary CD59 deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive cerebral atrophy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| COL4A1-related familial vascular leucoencephalopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| KCNQ2-related neonatal epileptic encephalopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Sodium channelopathy-related small fibre neuropathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Mitochondrial DNA depletion syndrome hepatocerebrorenal form |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Dystonia aphonia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Male emopamil-binding protein disorder with neurological defect |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Huntington disease-like syndrome due to C9ORF72 expansions |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Gemignani syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Congenital muscular dystrophy with intellectual disability and severe epilepsy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial episodic pain syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Inherited congenital spastic tetraplegia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Occipital pachygyria and polymicrogyria |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Congenital pontocerebellar hypoplasia type 10 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial adrenal hypoplasia with absent pituitary luteinising hormone |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Recessive mitochondrial ataxia syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Tremor, nystagmus, duodenal ulcer syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Thoracic dysplasia and hydrocephalus syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Parkinsonian pyramidal syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive myoclonic epilepsy type 8 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive myoclonic epilepsy type 6 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive myoclonic epilepsy type 5 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| AGel amyloidosis |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Ataxia with tapetoretinal degeneration syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cranio-cervical dystonia with laryngeal and upper limb involvement |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Adult-onset cervical dystonia DYT23 type |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| ADan amyloidosis |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Von Voss-Cherstvoy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypohidrosis-diabetes insipidus syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Malignant migrating partial seizures of infancy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial congenital mirror movements |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive spastic ataxia with leukoencephalopathy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Amyotrophic lateral sclerosis type 4 |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial infantile myoclonic epilepsy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Huntington disease-like 1 |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial mesial temporal lobe epilepsy with febrile seizures |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal dominant epilepsy with auditory features |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Multiple congenital anomalies, hypotonia, seizures syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Muscle eye brain disease with bilateral multicystic leukodystrophy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cobblestone lissencephaly without muscular or ocular involvement |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Infantile-onset autosomal recessive non progressive cerebellar ataxia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Obesity due to leptin receptor gene deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hyperekplexia epilepsy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Genetically determined myasthenia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Childhood-onset autosomal recessive myopathy with external ophthalmoplegia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Intellectual disability, hyperkinetic movement, truncal ataxia syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Amyotonia congenita |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked acrogigantism |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Huntington's chorea |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hereditary degenerative disease of central nervous system |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|