Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Familial infantile myoclonic epilepsy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Huntington disease-like 1 |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Familial mesial temporal lobe epilepsy with febrile seizures |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal dominant epilepsy with auditory features |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Multiple congenital anomalies, hypotonia, seizures syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Muscle eye brain disease with bilateral multicystic leukodystrophy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cobblestone lissencephaly without muscular or ocular involvement |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Infantile-onset autosomal recessive non progressive cerebellar ataxia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Obesity due to leptin receptor gene deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hyperekplexia epilepsy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Genetically determined myasthenia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Intellectual disability, hyperkinetic movement, truncal ataxia syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Amyotonia congenita |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Huntington's chorea |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hereditary degenerative disease of central nervous system |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Benign hereditary chorea |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Schwartz-Jampel syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Saldino-Mainzer dysplasia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Inherited optic neuropathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Meretoja syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Seckel syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
X-linked intellectual disability-psychosis-macroorchidism syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hereditary essential tremor |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Neu-Laxova syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
RAB18, member RAS oncogene family deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Marinesco-Sjögren syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Neurofibromatosis type 2 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Neurofibromatosis type 1 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Primary hyperaldosteronism, seizures, neurological abnormalities syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Diabetes, hypogonadism, deafness, intellectual disability syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Periventricular nodular heterotopia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal dominant progressive external ophthalmoplegia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive progressive external ophthalmoplegia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
X-linked progressive cerebellar ataxia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Primary inherited reading epilepsy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Neuropathy in association with hereditary ataxia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Intellectual disability, myopathy, short stature, endocrine defect syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Megalencephaly capillary malformation |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Proteus syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Bilateral frontoparietal polymicrogyria |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Familial spinal neurofibromatosis |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Type 3 lissencephaly |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hereditary ataxia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Acute neuronopathic Gaucher's disease |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Endosteal hyperostoses with cerebellar hypoplasia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Aspartylglucosaminuria |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Combined deficiency of sialidase AND beta galactosidase |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Choroid plexus carcinoma |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive distal hereditary motor neuropathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal dominant distal hereditary motor neuropathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
X-linked distal hereditary motor neuropathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
XK aprosencephaly syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Familial porencephaly |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Infantile-onset generalized dyskinesia with orofacial involvement |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
TBC1 domain containing kinase-related intellectual disability syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Fried syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Prenatal-onset spinal muscular atrophy with congenital bone fractures |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
X-linked immunoneurologic disorder |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Acyl-coenzyme A oxidase deficiency |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
X-linked panhypopituitarism |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Pontine autosomal dominant microangiopathy with leukoencephalopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hyperphenylalaninemia due to DnaJ heat shock protein family (Hsp40) member C12 deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Kallman syndrome with heart disease |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hereditary growth hormone deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Microcephalic cortical malformations, short stature due to rotatin deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Intellectual disability, epilepsy, extrapyramidal syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital ichthyosis, microcephalus, tetraplegia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cathepsin A-related arteriopathy, strokes, leukoencephalopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Lethal neonatal spasticity, epileptic encephalopathy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Amyotrophic lateral sclerosis type 1 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Amyotrophic lateral sclerosis type 3 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Amyotrophic lateral sclerosis type 8 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Amyotrophic lateral sclerosis type 9 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Familial congenital palsy of trochlear nerve |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Severe oculo-renal-cerebellar syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Amyotrophic lateral sclerosis type 10 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Polymicrogyria due to tubulin beta 2B class IIb mutation |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Progressive myoclonic epilepsy type 7 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cerebral ventriculomegaly, cystic kidney disease |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|