Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
X-linked intellectual disability with seizure and psoriasis syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Vici syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
X-linked intellectual disability with acromegaly and hyperactivity syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Microphthalmia with brain atrophy syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Acrootoocular syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Adult-onset dystonia parkinsonism |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Anonychia with microcephaly syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Aphalangy and syndactyly with microcephaly syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Ataxia with deafness and intellectual disability syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Athabaskan brainstem dysgenesis syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Brain calcification Rajab type |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Craniosynostosis and intracranial calcification syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cystic leukoencephalopathy without megalencephaly |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cerebrooculonasal syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Ehlers-Danlos syndrome with periventricular heterotopia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Filippi syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hall Riggs syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Short stature, pituitary and cerebellar defect and small sella turcica syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Developmental malformation, deafness, dystonia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Familial Alzheimer-like prion disease |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hydrocephalus, cardiac malformation, dense bone syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Brain dopamine-serotonin vesicular transport disease |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Huntington disease-like 2 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hydrocephalus with obesity and hypogonadism syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Lowry MacLean syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Lymphedema and cerebral arteriovenous anomaly syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Epiphyseal dysplasia, microcephalus, nystagmus syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Isotretinoin embryopathy-like syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hypogonadism with anosmia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Oculopalatocerebral syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Oculocerebrofacial syndrome Kaufman type |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital cataract, nephropathy, encephalopathy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital hereditary facial paralysis with variable hearing loss syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Congenital intrauterine infection-like syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cutaneous mastocytosis, short stature, hearing loss syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Galloway Mowat syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Severe X-linked mitochondrial encephalomyopathy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Severe X-linked intellectual disability Gustavson type |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Duane anomaly, myopathy, scoliosis syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Dystonia 16 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Familial caudal dysgenesis |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Infantile dystonia parkinsonism |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Inherited autonomic nervous system disorder |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Facial onset sensory and motor neuronopathy syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Ethylmalonic encephalopathy |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Endocrine-cerebro-osteodysplasia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Familial acute necrotizing encephalopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Macrostomia, preauricular tag, external ophthalmoplegia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Microlissencephaly micromelia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Microcephalic osteodysplastic dysplasia Saul Wilson type |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Non-progressive cerebellar ataxia with intellectual disability |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Renier Gabreels Jasper syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Sensorineural hearing loss, early graying, essential tremor syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Keratosis follicularis, dwarfism, cerebral atrophy syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Kufor Rakeb syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive posterior column ataxia and retinitis pigmentosa |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hereditary cerebral hemorrhage with amyloidosis |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Growth delay due to insulin-like growth factor type 1 deficiency |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Neuroectodermal melanolysosomal disease |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
McLeod neuroacanthocytosis syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Infantile osteopetrosis with neuroaxonal dysplasia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Infantile choroidocerebral calcification syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Hereditary hyperekplexia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
X-linked spasticity, intellectual disability, epilepsy syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal dominant striatal neurodegeneration |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive cerebellar ataxia Beauce type |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Microcephalic osteodysplastic primordial dwarfism types I and III |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive ataxia due to ubiquinone deficiency |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Pyridoxal 5-phosphate dependent epilepsy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Isolated optic nerve hypoplasia |
Is a |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Epileptic encephalopathy with global cerebral demyelination |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cataract, congenital heart disease, neural tube defect syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|
Cortical blindness, intellectual disability, polydactyly syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Existential restriction modifier |
|