Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Inherited spastic paresis |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Progressive sclerosing poliodystrophy |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Progressive sensory ataxia of Charolais |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Arrested hydrocephalus |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Dalmatian leukodystrophy |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Juvenile neuronal ceroid lipofuscinosis |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Azorean disease |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Parkinsonism due to heredodegenerative disorder (disorder) |
Due to |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
2 |
Chorea due to heredodegenerative disorder |
Due to |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
2 |
Parkinsonian pyramidal syndrome (disorder) |
Due to |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
2 |
Galactosylceramide beta-galactosidase deficiency |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Autosomal dominant late onset basal ganglia degeneration |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
HSMN IV |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Hereditary optic atrophy |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Alpha-N-acetylgalactosaminidase deficiency |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Metachromatic leukodystrophy, adult type |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Leigh's disease |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Hereditary cerebellar degeneration |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Hereditary spastic paraplegia |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Gerstmann-Straussler-Scheinker syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Pelizaeus-Merzbacher disease (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Cerebroretinal microangiopathy with calcifications and cysts |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
RNA polymerase III-related leukodystrophy |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Frontotemporal dementia with gene located on 3p11 (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
GRN-related frontotemporal dementia |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Adult onset autosomal dominant leukodystrophy (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Microphthalmia with brain atrophy syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Brain calcification Rajab type (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Craniosynostosis and intracranial calcification syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Familial Alzheimer-like prion disease (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Odontoleukodystrophy (disorder) |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Severe X-linked intellectual disability Gustavson type (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Facial onset sensory and motor neuronopathy syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Infantile choroidocerebral calcification syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Autosomal dominant striatal neurodegeneration (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Dermatoleukodystrophy |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Spastic paraparesis co-occurrent with deafness (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Familial Creutzfeldt-Jakob (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Behavioral variant of frontotemporal dementia (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Pelizaeus Merzbacher like disease (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Prion protein systemic amyloidosis (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Hypomyelination with brain stem and spinal cord involvement and leg spasticity (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Autosomal recessive cerebral atrophy |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Gemignani syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Progressive myoclonic epilepsy type 3 |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
ADan amyloidosis |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Amyotrophic lateral sclerosis type 4 |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Huntington disease-like 1 (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Hypotonia, speech impairment, severe cognitive delay syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder) |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
PRKAR1B-related neurodegenerative dementia with intermediate filaments |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Ferro-cerebro-cutaneous syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Fatal post-viral neurodegenerative disorder |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Wilson's disease |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Alexander disease |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Fatal familial insomnia |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Muscle eye brain disease with bilateral multicystic leukodystrophy |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Progressive cone-rod dystrophy |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Wolfram syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Familial dementia British type (disorder) |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Keratosis follicularis, dwarfism, cerebral atrophy syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Hereditary oculoleptomeningeal amyloid angiopathy |
Is a |
False |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Huntington's chorea |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Early onset parkinsonism and intellectual disability syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Autosomal dominant late onset Parkinson disease (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Vanishing white matter disease (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Progressive cerebellar ataxia with hypogonadism |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Autosomal recessive familial Parkinson disease |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Childhood-onset basal ganglia degeneration syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Ocular anomalies, axonal neuropathy, developmental delay syndrome |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
C11ORF73-related autosomal recessive hypomyelinating leukodystrophy (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Severe X-linked mitochondrial encephalomyopathy (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Combined oxidative phosphorylation defect type 27 |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Leucoencephalopathy with calcifications and cysts |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Infantile inflammatory bowel disease with neurological involvement (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Classical pantothenate kinase associated neurodegeneration |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Atypical pantothenate kinase associated neurodegeneration (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder) |
Is a |
True |
Hereditary degenerative disease of central nervous system |
Inferred relationship |
Some |
|