| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Congenital chorioretinal degeneration |
Is a |
False |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Aicardi's syndrome |
Is a |
False |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Spinocerebellar ataxia dysmorphism syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Hypotonia, speech impairment, severe cognitive delay syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Pelizaeus-Merzbacher disease, connatal variant |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Craniosynostosis and intracranial calcification syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Severe X-linked intellectual disability Gustavson type |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Encephalopathy, intracerebral calcification, retinal degeneration syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Combined immunodeficiency with faciooculoskeletal anomalies syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly |
Is a |
False |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Keratosis follicularis, dwarfism, cerebral atrophy syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Progressive epilepsy-intellectual disability syndrome Finnish type |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Pelizaeus-Merzbacher disease null syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Pelizaeus-Merzbacher disease in female carrier |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|
| Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome |
Is a |
True |
Congenital degeneration of nervous system |
Inferred relationship |
Existential restriction modifier |
|