Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Infantile cerebellar and retinal degeneration (disorder) |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
atrophie cérébrale et cérébelleuse infantile avec microcéphalie postnatale progressive |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Combined oxidative phosphorylation defect type 29 |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Progressive cerebello-cerebral atrophy (disorder) |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
paraplégie spastique héréditaire (trouble) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Episodic ataxia (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Myoclonic epilepsy myopathy sensory ataxia (disorder) |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Huntington disease-like syndrome |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
ataxie spinocérébelleuse type 36 |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 7 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 1 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 2 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 6 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 8 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 10 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 4 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Richards-Rundle syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Autosomal recessive cerebelloparenchymal disorder type 3 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 28 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
ataxie spinocérébelleuse type 29 |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 31 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
ataxie spinocérébelleuse type 15/16 |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 26 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 25 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 20 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 23 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 21 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 11 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 12 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 13 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
ataxie spinocérébelleuse type 14 |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 17 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
ataxie spinocérébelleuse type 18 |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 19 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 27 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 30 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 32 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 34 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 35 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 37 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 5 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
X-linked sideroblastic anemia with spinocerebellar ataxia |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
X-linked spinocerebellar ataxia type 3 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
X-linked spinocerebellar ataxia type 4 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar degeneration and corneal dystrophy syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Infantile onset spinocerebellar ataxia (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia dysmorphism syndrome |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 40 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Spinocerebellar ataxia type 38 (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Complicated hereditary spastic paraplegia |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
X-linked hereditary spastic paraplegia (disorder) |
est un(e) (attribut) |
False |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
ataxie spinocérébelleuse dominante |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary cerebellar degeneration |
Inferred relationship |
Some |
|