ophthalmoplegia

Preferred Label : ophthalmoplegia;

MeSH definition : 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.;

MeSH synonym : paralysis, oculomotor; ophthalmoplegias; oculomotor paralysis;

MeSH hyponym : external ophthalmoplegia; internal ophthalmoplegia; ophthalmoparesis; Internal Ophthalmoplegias; Ophthalmoplegia, Internal; Ophthalmoplegias, Internal; Ophthalmopareses; External Ophthalmoplegias; Ophthalmoplegia, External; Ophthalmoplegias, External;

MeSH annotation : do not confuse X ref OCULOMOTOR PARALYSIS with OCULOMOTOR NERVE PARALYSIS; do not confuse entry term OCULOMOTOR PARALYSIS with OCULOMOTOR NERVE PARALYSIS;

Wikipedia link : https://en.wikipedia.org/wiki/Ophthalmoparesis;

Details

Origin ID

D009886;

UMLS CUI

C0029089;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- EYE MUSCLE PARALYSIS [WHO-ART Preferred Term]
- External ophthalmoplegia [ICD-9 code]
- External ophthalmoplegia [HPO term]
- External ophthalmoplegia [MedDRA LLT]
- External ophthalmoplegia (disorder) [SNOMED CT concept]
- Internal ophthalmoplegia [PASCAL descriptor]
- Internal ophthalmoplegia [ICD-11 Subcategory]
- Internal ophthalmoplegia [HPO term]
- Internal ophthalmoplegia (disorder) [SNOMED CT concept]
- OCULOMOTOR PARALYSIS [WHO-ART Included Term]
- Ocular motor nerve palsies [ICD-11 Category]
- Oculomotor paralysis [MedDRA LLT]
- Ophthalmoparesis [ICD-11 Subcategory]
- Ophthalmoparesis [HPO term]
- Ophthalmoplegia externa [MedDRA LLT]
- Ophthalmoplegia interna [MedDRA LLT]
- Other paralytic strabismus [ICD-10 Sub-category (who)]
- Paralysis oculomotor [MedDRA LLT]
- Pseudoophthalmoplegia (disorder) [SNOMED CT concept]
- Rare oculomotor nerve disorder [ORDO Disease]
- Third nerve palsy [ICD-11 Subcategory]
- external ophthalmoplegia [SNOMED Notion]
- pseudoophthalmoplegia [SNOMED Notion]
Currated CISMeF NLP mapping
- OPHTHALMOPLEGIA [WHO-ART Included Term]
- Ophthalmoplegia [PASCAL descriptor]
- Ophthalmoplegia [ICD-11 More detail]
- Ophthalmoplegia [HPO term]
- Ophthalmoplegia [MedDRA Preferred Term]
- Ophthalmoplegia [NCIt concept]
- Ophthalmoplegia (disorder) [SNOMED CT concept]
- Ophthalmoplegia NOS [MedDRA LLT]
- ophthalmoplegia [DO Concept]
- ophthalmoplegia [Disease (Nov.)]
- ophthalmoplegia, nos [SNOMED Notion]
DO Cross reference
- ophthalmoplegia [DO Concept]
HPO term
- External ophthalmoplegia [HPO term]
- Internal ophthalmoplegia [HPO term]
- Ophthalmoparesis [HPO term]
- Ophthalmoplegia [HPO term]
Manual BTNT mappings - CISMeF
- Nuclear oculomotor paralysis [ORDO Disease]
- Supranuclear eye movement disorder [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Genetic neuro-ophthalmological disease [ORDO Disease]
- Neuro-ophthalmological disease [ORDO Disease]
Record concept(s)
- external ophthalmoplegia [MeSH concept]
- internal ophthalmoplegia [MeSH concept]
- ophthalmoparesis [MeSH concept]
- ophthalmoplegia [MeSH concept]
Related MeSH Supplementary Concept(s)
- CANOMAD syndrome [MeSH Supplementary Concept]
- adenine nucleotide translocator deficiency [MeSH Supplementary Concept]
- congenital fibrosis of the extraocular muscles [MeSH Supplementary Concept]
- external ophthalmoplegia, synergistic divergence, jaw winking, and oculocutaneous hypopigmentation [MeSH Supplementary Concept]
- fibrosis of extraocular muscles, congenital, 2 [MeSH Supplementary Concept]
- hamano tsukamoto syndrome [MeSH Supplementary Concept]
- inclusion body myopathy 3, autosomal dominant [MeSH Supplementary Concept]
- inclusion body myopathy, autosomal dominant [MeSH Supplementary Concept]
- minicore myopathy with external ophthalmoplegia [MeSH Supplementary Concept]
- motor neuron disease with dementia and ophthalmoplegia [MeSH Supplementary Concept]
- ocular myopathy with curare sensitivity [MeSH Supplementary Concept]
- oculomelic amyoplasia [MeSH Supplementary Concept]
- oculootoradial syndrome [MeSH Supplementary Concept]
- ophthalmoplegia totalis with ptosis and miosis [MeSH Supplementary Concept]
- ophthalmoplegia, external, and myopia [MeSH Supplementary Concept]
- ophthalmoplegia, familial static [MeSH Supplementary Concept]
- ophthalmoplegia, familial total, with iris transillumination [MeSH Supplementary Concept]
- ophthalmoplegia, progressive, with scrotal tongue and mental deficiency [MeSH Supplementary Concept]
- ophthalmoplegic neuromuscular disorder with abnormal mitochondria [MeSH Supplementary Concept]
- optic atrophy, deafness, ophthalmoplegia, and myopathy [MeSH Supplementary Concept]
- progressive external ophthalmoplegia with hypogonadism [MeSH Supplementary Concept]
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1 [MeSH Supplementary Concept]
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive [MeSH Supplementary Concept]
- schimke X-linked mental retardation syndrome [MeSH Supplementary Concept]
- sensory ataxic neuropathy, dysarthria, and ophthalmoparesis [MeSH Supplementary Concept]
- treft sanborn carey syndrome [MeSH Supplementary Concept]
- visceral myopathy familial external ophthalmoplegia [MeSH Supplementary Concept]
- wieacker syndrome [MeSH Supplementary Concept]
See also
- duane retraction syndrome [MeSH Descriptor]
- oculomotor nerve diseases [MeSH Descriptor]
Semantic type(s)
- Sign or Symptom [UMLS semantic type]
UMLS correspondences (same concept)
- EYE MUSCLE PARALYSIS [WHO-ART Preferred Term]
- Eye muscle paralysis [MedDRA LLT]
- Muscle paralysis eye [MedDRA LLT]
- OCULOMOTOR PARALYSIS [WHO-ART Included Term]
- OPHTHALMOPLEGIA [WHO-ART Included Term]
- Oculomotor paralysis [MedDRA LLT]
- Ophthalmoplegia [MedDRA Preferred Term]
- Ophthalmoplegia [HPO term]
- Ophthalmoplegia [PASCAL descriptor]
- Ophthalmoplegia [NCIt concept]
- Ophthalmoplegia (disorder) [SNOMED CT concept]
- Ophthalmoplegia NOS [MedDRA LLT]
- Paralysis extraocular muscle (s) [MedDRA LLT]
- Paralysis oculomotor [MedDRA LLT]
- Rare oculomotor nerve disorder [ORDO Disease]
- ophthalmoplegia [DO Concept]
- ophthalmoplegia [Disease (Nov.)]
- ophthalmoplegia, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- external ophthalmoplegia [Disease (Nov.)]
- internal ophthalmoplegia [Disease (Nov.)]
- ophthalmoparesis [Disease (Nov.)]

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