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Diseases

Ophthalmoplegia

ophthalmoplegia

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
Ophthalmoplegia
Standard Disease Name
ophthalmoplegia
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D009886
OMIM ID
MTHU008498|MTHU010326
UMLS ID
C0029089
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:Weakness or paralysis of at least one of the muscles controlling the movement of the eye. It results from degeneration of the muscles or the neural pathways involved in the eye movement. Representative disorders causing ophthalmoplegia include ocular myopathies and multiple sclerosis.|MSH2017_2016_08_12:Paralysis of one or more of the ocular muscles due to disorders of the eye muscles, neuromuscular junction, supporting soft tissue, tendons, or innervation to the muscles.|HPO2016_07_04:Paralysis of one or more extraocular muscles that are responsible for eye movements. [HPO:probinson]
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
04
NDUFS4
NADH:ubiquinone oxidoreductase subunit S4
NADH:ubiquinone oxidoreductase subunit S4
05
NDUFV1
NADH:ubiquinone oxidoreductase core subunit V1
NADH:ubiquinone oxidoreductase core subunit V1
06
OPA1
OPA1 mitochondrial dynamin like GTPase
OPA1 mitochondrial dynamin like GTPase
08
SCN4A
sodium voltage-gated channel alpha subunit 4
sodium voltage-gated channel alpha subunit 4