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Ontology Browser

Term:
Ophthalmoplegia, Familial Total, with Iris Transillumination (DOID:9005376)
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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 +   
distal arthrogryposis type 5  
exophthalmic ophthalmoplegia 
External Ophthalmoplegia and Myopia 
External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation 
Hamano Tsukamoto Syndrome 
Inclusion Body Myopathy 3, Autosomal Dominant  
internuclear ophthalmoplegia 
IVIC syndrome  
Miles-Carpenter syndrome  
Minicore Myopathy with External Ophthalmoplegia  
mitochondrial DNA depletion syndrome 11  
Motor Neuron Disease with Dementia and Ophthalmoplegia 
Ocular Myopathy with Curare Sensitivity 
Ophthalmoplegia Totalis with Ptosis and Miosis 
Ophthalmoplegia, Familial Static 
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  
Treft Sanborn Carey Syndrome 

Synonyms
Primary IDs: MESH:C563499 ;   RDO:0012741

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.