OCULOMOTOR PARALYSIS

Preferred Label : OCULOMOTOR PARALYSIS;

Origin ID

0133;

UMLS CUI

C0029089;

Automatic exact mappings (from CISMeF team)
- Ocular motor nerve palsies [ICD-11 Category]
- Ophthalmoplegia [HPO term]
- Third nerve palsy [ICD-11 Subcategory]
- ophthalmoplegia [DO Concept]
- ophthalmoplegia [MeSH Descriptor]
- ophthalmoplegia [MeSH concept]
Currated CISMeF NLP mapping
- Oculomotor paralysis [MedDRA LLT]
- Ophthalmoparesis [HPO term]
- Paralysis oculomotor [MedDRA LLT]
- Rare oculomotor nerve disorder [ORDO Disease]
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]
Semantic type(s)
- Sign or Symptom [UMLS semantic type]
UMLS correspondences (same concept)
- Eye muscle paralysis [MedDRA LLT]
- Muscle paralysis eye [MedDRA LLT]
- 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 [MeSH Descriptor]
- ophthalmoplegia [MeSH concept]
- ophthalmoplegia [DO Concept]
- ophthalmoplegia [Disease (Nov.)]
- ophthalmoplegia, nos [SNOMED Notion]