Welcome
{{ username}}
Message Center
{{ messageCount }} Messages
Go to Message Center
Watched Genes
{{$index + 1}}.
{{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Modify Subscription
Unsubscribe
Watched Ontology Terms
{{$index + 1}}.
{{ watchedTerm.term }} ({{watchedTerm.accId}})
Modify Subscription
Unsubscribe
{{gene.symbol}}:
{{ gene.description }}
×
Save List to My RGD
Create Name:
Description:
You must be logged in to use this feature
{{ loginError }}
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be sent to {{ username }}
{{geneWatchAttr}}
Analyze
Gene
Strain
QTL
List
×
Gene Annotator (Functional Annotation)
unavailable
Gene Annotator (Annotation Distribution)
unavailable
Variant Visualizer (Genomic Variants)
unavailble
Variant Visualizer (Genomic Variants)
unavailable
Gene Annotator (Functional Annotation)
Gene Annotator (Annotation Distribution)
Variant Visualizer (Genomic Variants)
InterViewer (Protein-Protein Interactions)
unavailable
Gviewer (Genome Viewer)
unavailable
Variant Visualizer (Damaging Variants) unavailble
Variant Visualizer (Damaging Variants)
unavailable
InterViewer (Protein-Protein Interactions)
GViewer (Genome Viewer)
Variant Visualizer (Damaging Variants)
Gene Annotator (Annotation Comparison)
unavailable
OLGA (Gene List Generator)
unavailable
Gene Annotator (Annotation Comparison)
OLGA (Gene List Generator)
Excel (Download)
MOET (Multi-Ontology Enrichement)
unavailable
GOLF (Gene-Ortholog Location Finder)
unavailable
MOET (Multi-Ontology Enrichement)
GOLF (Gene-Ortholog Location Finder)
x
Send Message
x
Send us a Message
Your email
Message
Send
Submit Data
|
Help
|
Video Tutorials
|
News
|
Publications
|
Download
|
REST API
|
Citing RGD
|
Contact
Home
Search RGD
Grant Resources
Citing RGD
About Us
Contact Us
Data
Genes
Variants
Community Projects
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
OntoMate (Literature Search)
JBrowse (Genome Browser)
Synteny Browser (VCMap)
Variant Visualizer
Multi-Ontology Enrichment (MOET)
Gene-Ortholog Location Finder (GOLF)
InterViewer (Protein-Protein Interactions)
PhenoMiner (Quatitative Phenotypes)
Gene Annotator
OLGA (Gene List Generator)
AllianceMine
GViewer (Genome Viewer)
Diseases
Aging & Age-Related Disease
Cancer & Neoplastic Disease
Cardiovascular Disease
Coronavirus Disease
Developmental Disease
Diabetes
Hematologic Disease
Immune & Inflammatory Disease
Infectious Disease
Liver Disease
Neurological Disease
Obesity & Metabolic Syndrome
Renal Disease
Respiratory Disease
Sensory Organ Disease
Phenotypes & Models
Find Models
Genetic Models
Autism Models
Rat PhenoMiner (Quantitative Phenotypes)
Chinchilla PhenoMiner
Expected Ranges (Quantitative Phenotype)
PhenoMiner Term Comparison
Hybrid Rat Diversity Panel
Phenotypes
Phenotypes in Other Animal Models
Animal Husbandry
Strain Medical Records
Phylogenetics
Strain Availability
Calendar
Rats 101
Submissions
Photo Archive
Pathways
Community
Rat Community Forum
Directory of Rat Laboratories
Video Tutorials
News
RGD Publications
RGD Presentations Archive
Nomenclature Guidelines
Resource Links
Laboratory Resources
Employment Resources
Advanced Search (OLGA)
Ontology Browser
Term:
internuclear ophthalmoplegia
(DOID:538)
Annotations:
Rat: (0)
Mouse: (0)
Human: (0)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (0)
Naked Mole-rat: (0)
Green Monkey: (0)
Parent Terms
Term With Siblings
Child Terms
ophthalmoplegia
+
strabismus
+
3MC syndrome 2
Adenine Nucleotide Translocator Deficiency
Alazami-Yuan Syndrome
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY
binocular vision disease
+
BROWN SYNDROME
CANOMAD Syndrome
chronic progressive external ophthalmoplegia
+
congenital fibrosis of the extraocular muscles
+
congenital myopathy 1B
congenital myopathy 6
conjugate gaze palsy
cyclotropia
Delayed Speech Development, with Facial Asymmetry, Strabismus, and Transverse Earlobe Crease
distal arthrogryposis type 5
Duane retraction syndrome
+
esotropia
+
exophthalmic ophthalmoplegia
exotropia
+
External Ophthalmoplegia and Myopia
External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation
Familial Static Ophthalmoplegia
Hamano Tsukamoto Syndrome
Hemifacial Hyperplasia with Strabismus
hypertropia
hypotropia
Impaired intellectual development, anterior maxillary protrusion, and strabismus
intermittent squint
internuclear ophthalmoplegia
IVIC syndrome
Krauss Herman Holmes Syndrome
McPherson Robertson Cammarano Syndrome
mechanical strabismus
+
Mehes Syndrome
mitochondrial DNA depletion syndrome 11
monofixation syndrome
Motor Neuron Disease with Dementia and Ophthalmoplegia
Ocular Myopathy with Curare Sensitivity
Ophthalmoplegia Totalis with Ptosis and Miosis
OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES
Ophthalmoplegia, Familial Total, with Iris Transillumination
Ophthalmoplegic Migraine
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy
paralytic squint
+
Progressive External Ophthalmoplegia with Hypogonadism
Progressive Ophthalmoplegia with Scrotal Tongue and Mental Deficiency
progressive supranuclear palsy
+
Ptosis, Strabismus, and Ectopic Pupils
Schimke X-Linked Mental Retardation Syndrome
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
Singh Chhaparwal Dhanda Syndrome
Treft Sanborn Carey Syndrome
Van Bogaert-Hozay Syndrome
Wieacker-Wolff syndrome
Synonyms
Exact Synonyms:
internuclear ophthalmoplegias
Xrefs:
ICD10CM:H51.2
;
ICD9CM:378.86
Definition Sources:
MESH:D015835