Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Acute neuronopathic Gaucher's disease |
Is a |
False |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Arginase deficiency |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Sialidosis |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Globoid cell leukodystrophy, late-onset |
Is a |
False |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Neuronal ceroid lipofuscinosis |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Gangliosidosis |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Niemann-Pick disease, type A (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Subacute neuronopathic Gaucher's disease |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Pelizaeus-Merzbacher disease (disorder) |
Is a |
False |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Deficiency of cerebroside-sulfatase |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Alexander's disease |
Is a |
False |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Niemann-Pick disease, type C, acute form |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Pyruvate carboxylase deficiency |
Is a |
False |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Deficiency of monoamine oxidase A (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Encephalopathy due to prosaposin deficiency (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Ganglioside GM3 synthase deficiency (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Thiamine-responsive encephalopathy (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Mucolipidosis type IV (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Deficiency of alpha-ketoglutarate dehydrogenase (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
3-phosphoglycerate dehydrogenase deficiency juvenile form (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
3-phosphoglycerate dehydrogenase deficiency infantile form (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Contiguous ABCD1 DXS1357E deletion syndrome (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Congenital cataract, hearing loss, severe developmental delay syndrome (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Lipoic acid synthetase deficiency (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Congenital muscular dystrophy with cerebellar involvement |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Congenital muscular dystrophy with intellectual disability |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Combined oxidative phosphorylation defect type 11 |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Navajo neurohepatopathy |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Combined oxidative phosphorylation defect type 30 |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Combined oxidative phosphorylation defect type 29 |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Combined oxidative phosphorylation defect type 27 |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Combined oxidative phosphorylation defect type 25 (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Combined oxidative phosphorylation defect type 23 |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|
Seizures, scoliosis, macrocephaly syndrome (disorder) |
Is a |
True |
Inherited metabolic disorder of nervous system |
Inferred relationship |
Some |
|