| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Cortical blindness, intellectual disability, polydactyly syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cyprus facial neuromusculoskeletal syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Coenzyme A synthase protein associated neurodegeneration (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hydrocephalus, tall stature, joint laxity syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Beta-propeller protein-associated neurodegeneration (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Epilepsy telangiectasia syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Myoclonus, cerebellar ataxia, deafness syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Absent tibia, polydactyly, arachnoid cyst syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Thyrocerebrorenal syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Stimmler syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Early-onset Lafora body disease (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Leukoencephalopathy, dystonia, motor neuropathy syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Pseudoprogeria syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Prion protein systemic amyloidosis (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephalus, digital anomaly, intellectual disability syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Isolated hereditary congenital facial paralysis (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Dandy-Walker malformation with postaxial polydactyly syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephalus, lymphedema, chorioretinopathy syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autism spectrum disorder, epilepsy, arthrogryposis syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Pyridoxine-dependent epilepsy (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cerebral folate transport deficiency (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| 2-methyl-3-hydroxybutyric aciduria (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Isolated follicle stimulating hormone deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cleft palate, large ears, small head syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive cerebellar ataxia with late-onset spasticity |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive myoclonic epilepsy with dystonia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Spectrin-associated autosomal recessive cerebellar ataxia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial dyskinesia and facial myokymia (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hot water reflex epilepsy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Spastic ataxia with congenital miosis |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Deafness, encephaloneuropathy, obesity, valvulopathy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial hyperprolactinemia |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypotonia, speech impairment, severe cognitive delay syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial cortical myoclonus |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Fragile X associated tremor ataxia syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Episodic ataxia type 7 (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Episodic ataxia type 6 (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Episodic ataxia type 4 (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Episodic ataxia type 3 (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Episodic ataxia type 5 (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Agenesis of corpus callosum and abnormal genitalia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Oro-facial digital syndrome type 14 |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Pachygyria, intellectual disability, epilepsy syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Myosclerosis (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Action myoclonus renal failure syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial focal epilepsy with variable foci |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Rolandic epilepsy, speech dyspraxia syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Familial multiple benign meningioma (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Pitt-Hopkins syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Diencephalic mesencephalic junction dysplasia (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked non progressive cerebellar ataxia (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypomyelination neuropathy arthrogryposis syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Moebius syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypermanganesemia with dystonia (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Ataxia pancytopenia syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| CLCN2-related leukoencephalopathy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Odontoleukodystrophy (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Adult onset autosomal dominant leukodystrophy (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| RNA polymerase III-related leukodystrophy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Pelizaeus Merzbacher like disease (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cerebroretinal vasculopathy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Dermatoleukodystrophy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephalic primordial dwarfism Alazami type (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Autosomal recessive chorioretinopathy and microcephaly syndrome (disorder) |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephalic primordial dwarfism Dauber type |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Benign familial mesial temporal lobe epilepsy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked cerebral, cerebellar, coloboma syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked parkinsonism with spasticity syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephaly, thin corpus callosum, intellectual disability syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|