Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
neuropathie autonome diabétique liée au diabète sucré de type 2 |
Is a |
False |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Autonomic neuropathy due to diabetes mellitus (disorder) |
Is a |
False |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Diabetic mononeuropathy |
Is a |
False |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Mononeuritis multiplex with diabetes mellitus |
Is a |
False |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Entrapment syndrome due to amyloid (disorder) |
Is a |
False |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Diabetic autonomic neuropathy associated with type 1 diabetes mellitus |
Is a |
False |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Radiculoplexus neuropathy due to diabetes mellitus (disorder) |
Is a |
False |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Peripheral neuropathy of upper limb due to metabolic disorder (disorder) |
Is a |
True |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Diabetic peripheral neuropathy |
Is a |
True |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
A rare mitochondrial disease characterized by adult onset of the triad of sensory ataxic neuropathy, dysarthria, and ophthalmoparesis. Additional signs and symptoms are highly variable and include myopathy, seizures, and hearing loss, among others. Brain imaging may show cerebellar white matter abnormalities and/or bilateral thalamic lesions. |
Is a |
True |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome is a rare mitochondrial disease due to a defect in coenzyme Q10 biosynthesis that manifests with a broad spectrum of signs and symptoms which may include: neonatal lactic acidosis, global developmental delay, tonus disorder, seizures, reduced spontaneous movements, ventricular hypertrophy, bradycardia, renal tubular dysfunction with massive lactic acid excretion in urine, severe biochemical defect of respiratory chain complexes II/III when assayed together and deficiency of coenzyme Q10 in skeletal muscle. Cerebral and cerebellar atrophy can be seen on magnetic resonance imaging and multiple choroid plexus cysts and symmetrical hyperechoic signal alterations in basal ganglia have been observed on ultrasound. |
Is a |
True |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Deafness-encephaloneuropathy-obesity-valvulopathy syndrome is a rare mitochondrial disease with marked clinical variability typically characterized by encephalomyopathy, kidney disease (nephrotic syndrome), optic atrophy, early-onset deafness, pancytopenia, obesity, and cardiac disease (valvulopathy). Additionally, macrocephaly, intellectual disability, hyperlactatemia, elevated lactate/pyruvate ratio, insulin-dependent diabetes, livedo reticularis, liver dysfunction and seizures have also been associated. |
Is a |
True |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Neuropathic arthropathy due to diabetes mellitus (disorder) |
Is a |
False |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|
Radiculopathy due to metabolic disorder |
Is a |
True |
Peripheral neuropathy due to metabolic disorder (disorder) |
Inferred relationship |
Some |
|