| Inbound Relationships | 
Type | 
Active | 
Source | 
Characteristic | 
Refinability | 
Group | 
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital hemiplegia (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Leber's optic atrophy | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Pyridoxine-dependent epilepsy (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Spinal hydromeningocele | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| X-linked distal arthrogryposis multiplex congenita (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Microcephaly-capillary malformation syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Odontotrichomelic syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital syphilitic meningitis | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Microphthalmia with brain atrophy syndrome (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital sixth nerve palsy (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Microcephalus microcornea syndrome of Seemanova type (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital atrophy of optic nerve (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Malformation of central nervous system of fetus (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Spondyloenchondromatosis with basal ganglia calcification (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| hereditaire nefrogene diabetes insipidus (aandoening) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Cervical hypertrichosis and peripheral neuropathy syndrome (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Late congenital neurosyphilis | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Primary congenital glaucoma (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Progressive congenital rubella encephalomyelitis | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Hemianencephaly | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Marinesco-Sjögren syndrome (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Frontoethmoidal encephalocele | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital cerebral hernia | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital porencephalic cyst (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital quadriplegia | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Ethylmalonic encephalopathy (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital combined disorder of muscle and peripheral nerve (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital nuclear ophthalmoplegia | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital anomaly of nervous system | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital anosmia | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Neu-Laxova syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Acrootoocular syndrome (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| FOXG1 syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Ataxia-telangiectasia syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Dementia with Down syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Thyrocerebrorenal syndrome | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Menkes kinky-hair syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| X-linked distal spinal muscular atrophy type 3 (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| X-linked non progressive cerebellar ataxia (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| X-linked hereditary motor and sensory neuropathy | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Hypotonia, speech impairment, severe cognitive delay syndrome (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| X-linked sideroblastic anemia with spinocerebellar ataxia | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Action myoclonus renal failure syndrome | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Spastic ataxia with congenital miosis | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| X-gebonden acromegalie | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Spectrin-associated autosomal recessive cerebellar ataxia | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type D | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Familial hyperprolactinemia | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Charcot-Marie-Tooth disease type 4 (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type C (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital meningocele | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Rolandic epilepsy, speech dyspraxia syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type A (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Autosomal dominant slowed nerve conduction velocity | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Familial focal epilepsy with variable foci | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Autosomal dominant congenital benign spinal muscular atrophy | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| HIVEP2-related intellectual disability | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital trigeminal anesthesia (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Progressive external ophthalmoplegia, myopathy, emaciation syndrome | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| 5q31.3 microdeletion syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Myosclerosis (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| hydromeningocele | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Multiple congenital anomalies, hypotonia, seizures syndrome type 2 | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Pitt-Hopkins-achtig syndroom (aandoening) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Late congenital syphilitic polyneuropathy (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Infantile spasm and broad thumb syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Congenital Horner syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Jawad syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Ptosis and vocal cord paralysis syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (disorder) | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome | 
Is a | 
True | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Aganglionosis of large intestine (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Familial congenital palsy of trochlear nerve (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  | 
| Hirschsprung disease, ganglioneuroblastoma syndrome (disorder) | 
Is a | 
False | 
Congenital neurological disorder (disorder) | 
Inferred relationship | 
Some | 
  |