Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
syndrome de Schwartz-Jampel (trouble) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Saldino-Mainzer dysplasia |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Inherited optic neuropathy |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Meretoja syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
nanisme à tête d'oiseau |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
PPM-X syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Hereditary essential tremor |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Neu-Laxova syndrome |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
RAB18, member RAS oncogene family deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
syndrome de Marinesco-Sjögren |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Neurofibromatosis type 2 |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Neurofibromatosis type 1 |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Woodhouse Sakati syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Periventricular nodular heterotopia |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Autosomal dominant progressive external ophthalmoplegia (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Autosomal recessive progressive external ophthalmoplegia |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
X-linked progressive cerebellar ataxia |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Primary inherited reading epilepsy |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
myoclonie photo-induite, diabète sucré, surdité, néphropathie et dysfonctionnement cérébral |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Neuropathy in association with hereditary ataxia |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Intellectual disability, myopathy, short stature, endocrine defect syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
macrocéphalie, malformation capillaire |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Proteus syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Bilateral frontoparietal polymicrogyria (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Familial spinal neurofibromatosis |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Type 3 lissencephaly |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Leucodystrophy without a known biochemical basis |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Hereditary ataxia (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Acute neuronopathic Gaucher's disease |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Endosteal hyperostoses with cerebellar hypoplasia |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
aspartylglucosaminurie (trouble) |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Combined deficiency of sialidase AND beta galactosidase |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Choroid plexus carcinoma |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Autosomal recessive distal hereditary motor neuropathy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Autosomal dominant distal hereditary motor neuropathy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
X-linked distal hereditary motor neuropathy |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
XK aprosencephaly syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Familial porencephaly (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
MARCH syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Infantile-onset generalised dyskinesia with orofacial involvement |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
RERE-related neurodevelopmental syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
TBCK-related intellectual disability syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Fried syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Prenatal-onset spinal muscular atrophy with congenital bone fractures (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
syndrome immuno-neurologique lié à l'X |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Acyl-coenzyme A oxidase deficiency (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
X-linked panhypopituitarism (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Pontine autosomal dominant microangiopathy with leukoencephalopathy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Hyperphenylalanineaemia due to DNAJC12 deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Kallman syndrome with heart disease (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Hereditary growth hormone deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Intellectual disability, epilepsy, extrapyramidal syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Cathepsin A-related arteriopathy, strokes, leucoencephalopathy |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Amyotrophic lateral sclerosis type 1 |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Amyotrophic lateral sclerosis type 3 |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Amyotrophic lateral sclerosis type 8 |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Amyotrophic lateral sclerosis type 9 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Familial congenital palsy of trochlear nerve (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Severe oculo-renal-cerebellar syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Amyotrophic lateral sclerosis type 10 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Polymicrogyria due to TUBB2B mutation |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Progressive myoclonic epilepsy type 7 |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Cerebral ventriculomegaly, cystic kidney disease |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Primary dystonia DYT27 type |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Giant axonal neuropathy |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Prune exopolyphosphatase 1-related neurological syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Progressive myoclonic epilepsy type 9 |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
PCNA-related progressive neurodegenerative photosensitivity syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Lethal brain and heart developmental defects syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Duane retraction syndrome with congenital deafness |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
CNTNAP2-related developmental and epileptic encephalopathy |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Hereditary continuous muscle fiber activity |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Benign familial neonatal-infantile seizures (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Congenital isolated adrenocorticotropic hormone deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Inherited metabolic disorder of nervous system |
est un(e) (attribut) |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
Autosomal dominant late onset basal ganglia degeneration |
est un(e) (attribut) |
False |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|