| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Spinocerebellar ataxia dysmorphism syndrome |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| syndrome d'hypotonie-trouble sévère du langage-retard cognitif sévère |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Pelizaeus-Merzbacher disease, connatal variant (disorder) |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Craniosynostosis and intracranial calcification syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Severe X-linked intellectual disability Gustavson type (disorder) |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| syndrome d'ataxie cérébelleuse, déficience intellectuelle, atrophie optique, anomalies cutanées |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| atrophie cérébrale et cérébelleuse infantile avec microcéphalie postnatale progressive |
est un(e) (attribut) |
False |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder) |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Keratosis follicularis, dwarfism, cerebral atrophy syndrome |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Neuronal ceroid lipofuscinosis 8 |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Pelizaeus-Merzbacher disease null syndrome |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Pelizaeus-Merzbacher disease in female carrier |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| PCNA-related progressive neurodegenerative photosensitivity syndrome |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Aicardi's syndrome |
est un(e) (attribut) |
False |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Congenital chorioretinal degeneration |
est un(e) (attribut) |
False |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|
| Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Some |
|