| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Hirschsprung disease, ganglioneuroblastoma syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Mitochondrial DNA depletion syndrome hepatocerebrorenal form | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital muscular dystrophy with intellectual disability and severe epilepsy | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Inherited congenital spastic tetraplegia | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital sacral meningocele | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Severe intellectual disability, progressive spastic diplegia syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Recessive mitochondrial ataxia syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Familial congenital mirror movements | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| PPM-X syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Gillespie syndrome | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| X-linked acrogigantism due to Xq26 microduplication | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Saldino-Mainzer dysplasia | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital central hypoventilation | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Alopecia, epilepsy, intellectual disability syndrome Moynahan type | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| congenitale uitval van nervus facialis | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Neurocutaneous melanosis | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Combined deficiency of sialidase AND beta galactosidase | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital cataract with ataxia and deafness syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Autosomal recessive Charcot-Marie-Tooth disease type 2 | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Aspartylglucosaminuria | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Hereditary cavernous hemangioma of brain (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Neurocutaneous syndrome | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Encephalocraniocutaneous lipomatosis | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Microcephalus, complex motor and sensory axonal neuropathy syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital isolated growth hormone deficiency | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Lipoma due to neurospinal dysraphism | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Fried syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Intellectual disability, spasticity, ectrodactyly syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Acyl-CoA oxidase deficiency | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Macrocephaly with spastic paraplegia and dysmorphism syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Allan-Herndon-Dudley syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Severe X-linked mitochondrial encephalomyopathy (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Spastic paraplegia, nephritis, deafness syndrome (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| X-linked neurodegenerative syndrome Bertini type (disorder) | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Progressive congenital rubella encephalitis (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Christianson syndrome | Is a | False | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Prenatal-onset spinal muscular atrophy with congenital bone fractures (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital palsy of trochlear nerve (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital oculomotor nerve palsy (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital fibrosis syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital horizontal gaze palsy (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital isolated adrenocorticotropic hormone deficiency (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Maroteaux-Lamy syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Amyotonia congenita | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Schwartz-Jampel syndrome | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| GM1 gangliosidosis | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Deafness, encephaloneuropathy, obesity, valvulopathy syndrome | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Contiguous ABCD1 DXS1357E deletion syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital cataract, hearing loss, severe developmental delay syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Encephalopathy due to prosaposin deficiency (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Ganglioside GM3 synthase deficiency (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Thiamine-responsive encephalopathy (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Sialidosis type 1 (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Mucolipidosis type IV (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Deficiency of alpha-ketoglutarate dehydrogenase (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| 3-phosphoglycerate dehydrogenase deficiency juvenile form (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| 3-phosphoglycerate dehydrogenase deficiency infantile form (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Lipoic acid synthetase deficiency (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Progressive myoclonic epilepsy type 3 | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital muscular dystrophy with intellectual disability | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Combined oxidative phosphorylation defect type 11 | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Navajo neurohepatopathy | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital myasthenic syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Multiple mitochondrial dysfunctions syndrome type 3 | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Megaconial congenital muscular dystrophy | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital insensitivity to pain with severe intellectual disability (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Albinism with deafness syndrome (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital axonal neuropathy with encephalopathy | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital pseudopapilledema (disorder) | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Oculocerebrodental syndrome | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Congenital hydrocephalus caused by toxoplasmosis | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Encephalocele | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  | 
| Dysequilibrium syndrome | Is a | True | Congenital neurological disorder (disorder) | Inferred relationship | Some |  |