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Diseases

Polyneuropathy

polyneuropathy

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Polyneuropathy
Standard Disease Name
polyneuropathy
MeSH Tree
No data
ICD-10
A69.22|G62.9

Identifiers

DO ID
No data
MeSH ID
D011115
OMIM ID
MTHU038003
UMLS ID
C0152025
HPO ID
No data

Description and Extensions

Description
MSH2017_2016_08_12:Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance.|HPO2016_07_04:A generalized disorder of peripheral nerves. [HPO:curators]|CHV2011_02:a nerve disease where many peripheral nerves are affected|CHV2011_02:a nerve disease where many peripheral nerves are affected
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
06
OPA1
OPA1 mitochondrial dynamin like GTPase
OPA1 mitochondrial dynamin like GTPase