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Ontology Browser

Motor Neuron Disease with Dementia and Ophthalmoplegia (DOID:9003543)
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Parent Terms Term With Siblings Child Terms
dementia +     
ophthalmoplegia +     
Adenine Nucleotide Translocator Deficiency 
AIDS Dementia Complex  
Alzheimer's disease +   
amyotrophic lateral sclerosis +   
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1  
Ataxia with Myoclonic Epilepsy and Presenile Dementia 
CANOMAD Syndrome 
Cerebral Amyloidosis with Spongiform Encephalopathy +   
chronic progressive external ophthalmoplegia +   
Congenital Arthrogryposis with Anterior Horn Cell Disease  
congenital fibrosis of the extraocular muscles +   
Creutzfeldt-Jakob disease +   
deafness-dystonia-optic neuronopathy syndrome  
Dementia/Parkinsonism with Non-Alzheimer Amyloid Plaques 
Diffuse Neurofibrillary Tangles with Calcification 
distal arthrogryposis type 5  
exophthalmic ophthalmoplegia 
External Ophthalmoplegia and Myopia 
External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation 
Frontotemporal Lobar Degeneration +   
Hamano Tsukamoto Syndrome 
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance 
Huntington's disease +   
Huntington's disease-like 2  
Inclusion Body Myopathy 3, Autosomal Dominant  
internuclear ophthalmoplegia 
ITM2B-related cerebral amyloid angiopathy 2  
IVIC syndrome  
juvenile amyotrophic lateral sclerosis with dementia 
Kluver-Bucy syndrome +  
Kohlschutter-Tonz syndrome  
lateral sclerosis 
Lewy body dementia +   
MAST syndrome  
Miles-Carpenter syndrome  
Minicore Myopathy with External Ophthalmoplegia  
mitochondrial DNA depletion syndrome 11  
motor neuritis +   
Motor Neuron Disease with Dementia and Ophthalmoplegia 
nonparalytic poliomyelitis 
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 
poliomyelitis +   
Presenile Dementia, Kraepelin Type 
Primary Lateral Sclerosis Juvenile  
Primary Progressive Aphasia +   
progressive bulbar palsy +   
Progressive External Ophthalmoplegia with Hypogonadism 
progressive muscular atrophy  
Progressive Ophthalmoplegia with Scrotal Tongue and Mental Deficiency 
progressive supranuclear palsy +   
pseudobulbar palsy +  
Schimke X-Linked Mental Retardation Syndrome 
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis  
Spastic Paraplegia, Optic Atrophy, and Dementia 
spinal muscular atrophy +   
Treft Sanborn Carey Syndrome 
vascular dementia +   
Wright Dyck Syndrome 

Primary IDs: MESH:C563954 ;   RDO:0013071

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