| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| 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 (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal dominant epilepsy with auditory features (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) |
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 (disorder) |
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 (disorder) |
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 (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Amyotonia congenita |
Is a |
True |
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 |
|
| Benign hereditary chorea |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Schwartz-Jampel syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Saldino-Mainzer dysplasia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Inherited optic neuropathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| syndrome de Meretoja |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Seckel syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| PPM-X syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hereditary essential tremor |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Neu-Laxova syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| RAB18, member RAS oncogene family deficiency (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Marinesco-Sjögren syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Neurofibromatosis type 2 |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Neurofibromatosis type 1 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Woodhouse Sakati syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Periventricular nodular heterotopia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal dominant progressive external ophthalmoplegia (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive progressive external ophthalmoplegia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked progressive cerebellar ataxia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Primary inherited reading epilepsy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Neuropathy in association with hereditary ataxia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Intellectual disability, myopathy, short stature, endocrine defect syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Megalencephaly capillary malformation |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Proteus syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Bilateral frontoparietal polymicrogyria (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial spinal neurofibromatosis |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Type 3 lissencephaly |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hereditary ataxia (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Acute neuronopathic Gaucher's disease |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Endosteal hyperostoses with cerebellar hypoplasia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Aspartylglucosaminuria |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Combined deficiency of sialidase AND beta galactosidase |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Choroid plexus carcinoma |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive distal hereditary motor neuropathy (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal dominant distal hereditary motor neuropathy (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked distal hereditary motor neuropathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| XK aprosencephaly syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial porencephaly (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| MARCH syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Infantile-onset generalised dyskinesia with orofacial involvement |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| RERE-related neurodevelopmental syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| TBCK-related intellectual disability syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Fried syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Prenatal-onset spinal muscular atrophy with congenital bone fractures (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked immunoneurologic disorder (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Acyl-CoA oxidase deficiency |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked panhypopituitarism (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Pontine autosomal dominant microangiopathy with leukoencephalopathy (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hyperphenylalanineaemia due to DNAJC12 deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Kallman syndrome with heart disease (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hereditary growth hormone deficiency (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Intellectual disability, epilepsy, extrapyramidal syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cathepsin A-related arteriopathy, strokes, leucoencephalopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Amyotrophic lateral sclerosis type 1 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Amyotrophic lateral sclerosis type 3 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Amyotrophic lateral sclerosis type 8 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Amyotrophic lateral sclerosis type 9 (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial congenital palsy of trochlear nerve (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Severe oculo-renal-cerebellar syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Amyotrophic lateral sclerosis type 10 (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Polymicrogyria due to TUBB2B mutation |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive myoclonic epilepsy type 7 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cerebral ventriculomegaly, cystic kidney disease |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|