Preferred Name

Ophthalmoplegia

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C79697

code

C79697

DEFINITION

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.

FULL_SYN

Ophthalmoplegia

label

Ophthalmoplegia

Legacy Concept Name

Ophthalmoplegia

Preferred_Name

Ophthalmoplegia

prefixIRI

Thesaurus:C79697

prefLabel

Ophthalmoplegia

Semantic_Type

Finding

UMLS_CUI

C4011453

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99208

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU008498 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/HP_0000602 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/MESH/D009886 Medical Subject Headings / 医学主题词表 LOOM
http://purl.obolibrary.org/obo/MONDO_0003425 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/DOID_539 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_539 Human Disease Ontology / 人类疾病本体 LOOM