Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
ophthalmoplegia +     
Adenine Nucleotide Translocator Deficiency 
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY  
CANOMAD Syndrome 
chronic progressive external ophthalmoplegia +   
congenital fibrosis of the extraocular muscles +   
congenital myopathy 1B  
congenital myopathy 6  
distal arthrogryposis type 5  
exophthalmic ophthalmoplegia 
External Ophthalmoplegia and Myopia 
External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation 
Familial Static Ophthalmoplegia 
Hamano Tsukamoto Syndrome 
internuclear ophthalmoplegia 
IVIC syndrome  
Miles-Carpenter syndrome +   
mitochondrial DNA depletion syndrome 11  
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 
Progressive External Ophthalmoplegia with Hypogonadism 
Progressive Ophthalmoplegia with Scrotal Tongue and Mental Deficiency 
progressive supranuclear palsy +   
Schimke X-Linked Mental Retardation Syndrome 
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis  
thyrotoxic exophthalmos 
Treft Sanborn Carey Syndrome 

Synonyms
Primary IDs: RDO:9003017
Xrefs: ICD9CM:376.22

paths to the root