Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Lumbosacral plexus neuropathy |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Motor neuropathy with multiple conduction block |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Family history of neuropathy (situation) |
Associated finding |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
1 |
Family history of neuropathy (situation) |
Associated finding |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
1 |
Family history of neuropathy (situation) |
Associated finding |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
1 |
Paraneoplastic neuropathy |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Nerve plexus disorder |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Superior oblique myokymia |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Congenital end-plate acetylcholinesterase deficiency |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Neuropathy due to unstable diabetes mellitus type 1 (disorder) |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Late congenital syphilitic polyneuropathy |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Neuropathy associated with endocrine disorder |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Neuropathy caused by isoniazid |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Xeroderma pigmentosum/Cockayne syndrome complex (XP/CS complex) is characterized by the cutaneous features of xeroderma pigmentosum (XP) together with the systemic and neurological features of Cockayne syndrome. |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Neuropathy due to nutritional deficiency (disorder) |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Neuropathy caused by heavy metal (disorder) |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Hypomyelination neuropathy-arthrogryposis syndrome is a rare, genetic, limb malformation syndrome characterized by multiple congenital distal joint contractures (including talipes equinovarus and both proximal and distal interphalangeal joint contractures of the hands) and very severe motor paralysis at birth (i.e. lack of swallowing, autonomous respiratory function and deep tendon reflexes), leading to death within first 3 months of life. Fetal hypo- or akinesia, late-onset polyhydramnios and dramatically reduced, or absent, motor nerve conduction velocities (<10 m/s) are frequently associated. Nerve ultrastructural morphology shows severe abnormalities of the nodes of Ranvier and myelinated axons. |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Leucodystrophy |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Vagus nerve laryngeal paralysis |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Postherpetic neuralgia |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Segmental neuralgia as late effect of traumatic injury |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Immune-mediated neuropathy |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Nerve palsy |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Postinfectious neuralgia |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Fibrolipomatous hamartoma of nerve (disorder) |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Neuralgia with AIDS (acquired immunodeficiency syndrome) |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Neuralgia co-occurrent with human immunodeficiency virus infection |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Lipoma of nerve |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Compression injury of nerve |
Is a |
False |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Erectile dysfunction due to neuropathy |
Due to |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
1 |
Iatrogenic neuropathy (disorder) |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Disorder of nerve due to metabolic disease (disorder) |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Neuropathy due to obesity |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Optic chiasm disorder |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Hereditary continuous muscle fiber activity is a rare, non-dystrophic myopathy characterized by generalized myokymia and increased muscle tone associated with delayed motor milestones, leg stiffness, spastic gait, hyperreflexia and Babinski sign. Symptoms may be worsened by febrile illness or anesthesia. |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Ophthalmoplegia due to neuropathy (disorder) |
Due to |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
3 |
Injection site paresthesia |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Impairment of motor nerve function as a complication of cutaneous surgery |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Perineural lipomatosis (disorder) |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Disease caused by homozygous mutation in the prosaposin gene (PSAP) on chromosome 10q22. The disease is genetically distinct from Krabbe disease. Clinical features include onset in infancy with respiratory and neurologic involvement. |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Neuropathy caused by ionising radiation |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|
Congenital absence of myelination of peripheral nerve (disorder) |
Is a |
True |
Neuropathy (disorder) |
Inferred relationship |
Some |
|