| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Primary dystonia DYT27 type |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Giant axonal neuropathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Prune exopolyphosphatase 1-related neurological syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Progressive myoclonic epilepsy type 9 |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| PCNA-related progressive neurodegenerative photosensitivity syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Lethal brain and heart developmental defects syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Duane retraction syndrome with congenital deafness |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| CNTNAP2-related developmental and epileptic encephalopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Hereditary continuous muscle fiber activity |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Benign familial neonatal-infantile seizures (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Congenital isolated adrenocorticotropic hormone deficiency (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| PYCR2-related microcephaly, progressive leucoencephalopathy |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| NDE1-related microhydranencephaly |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Cerebellar-facial-dental syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| EMILIN-1-related connective tissue disease |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Benign familial infantile epilepsy (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Albinism with deafness syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Oculocerebrodental syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Congenital leptin deficiency |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Megalencephaly, severe kyphoscoliosis, overgrowth syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Polyendocrine polyneuropathy syndrome (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Neuroferritinopathy (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder) |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|
| Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome |
Is a |
True |
Hereditary disorder of nervous system |
Inferred relationship |
Some |
|