Ophthalmoplegia [oftalmoplegie]
- Terms
-
oftalmoparéza
ophthalmoparesis
ophthalmoplegia
ophthalmoplegia externa
ophthalmoplegia interna
-
External Ophthalmoplegia
Internal Ophthalmoplegia
Oculomotor Paralysis
Ophthalmoparesis
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.
- Annotation
- do not confuse entry term OCULOMOTOR PARALYSIS with OCULOMOTOR NERVE PARALYSIS
- DUI
- D009886 MeSH Browser
- CUI
- M0015332
- History note
- 1979; was OCULOMOTOR PARALYSIS 1963-1978
- Online note
- use OPHTHALMOPLEGIA to search OCULOMOTOR PARALYSIS 1966-78
- Public note
- 1979; was OCULOMOTOR PARALYSIS 1963-1978
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 2
- CO
- complications 2
- CN
- congenital
- DI
- diagnosis 5
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology 19
- GE
- genetics 3
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 2
- PP
- physiopathology 2
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation 1
- SU
- surgery 2
- TH
- therapy 2
- UR
- urine
- VE
- veterinary
- VI
- virology
CANOMAD syndrome Disease MeSH Browser
Fibrosis Of Extraocular Muscles, Congenital, 2 Disease MeSH Browser
Hamano Tsukamoto syndrome Disease MeSH Browser
Inclusion Body Myopathy 3, Autosomal Dominant Disease MeSH Browser
Inclusion body myopathy, autosomal dominant Disease MeSH Browser
Minicore Myopathy with External Ophthalmoplegia Disease MeSH Browser
Motor Neuron Disease with Dementia and Ophthalmoplegia Disease MeSH Browser
Ocular Myopathy with Curare Sensitivity Disease MeSH Browser
Oculomelic amyoplasia Disease MeSH Browser
Oculootoradial syndrome Disease MeSH Browser
Ophthalmoplegia Totalis with Ptosis and Miosis Disease MeSH Browser
Ophthalmoplegia, External, and Myopia Disease MeSH Browser
Ophthalmoplegia, Familial Static Disease MeSH Browser
Ophthalmoplegia, Familial Total, with Iris Transillumination Disease MeSH Browser
Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency Disease MeSH Browser
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria Disease MeSH Browser
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy Disease MeSH Browser
Progressive External Ophthalmoplegia With Hypogonadism Disease MeSH Browser
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Disease MeSH Browser
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Disease MeSH Browser
Schimke X-linked mental retardation syndrome Disease MeSH Browser
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Disease MeSH Browser
Treft Sanborn Carey syndrome Disease MeSH Browser
Wieacker syndrome Disease MeSH Browser
congenital fibrosis of the extraocular muscles Disease MeSH Browser
external ophthalmoplegia, synergistic divergence, jaw winking, and oculocutaneous hypopigmentation Disease MeSH Browser