Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
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)
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
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
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:
Parent Terms Term With Siblings Child Terms
aceruloplasminemia 
Alpers syndrome 
Ataxia - oculomotor apraxia type 1 
Ataxia with vitamin E deficiency 
Ataxia-telangiectasia 
Atypical progressive supranuclear palsy +  
autosomal dominant cerebellar ataxia type I +   
autosomal dominant cerebellar ataxia type II 
autosomal dominant cerebellar ataxia type III +  
autosomal dominant cerebellar ataxia type IV +  
autosomal dominant optic atrophy +  
autosomal recessive optic atrophy 
cerebrotendinous xanthomatosis 
choroidal sclerosis +  
Chédiak-Higashi syndrome 
Classical progressive supranuclear palsy 
CLN1 disease 
CLN11 disease 
CLN13 disease 
CLN2 disease 
CLN3 disease 
CLN4A disease 
CLN4B disease 
CLN5 disease 
CLN6 disease 
CLN7 disease 
CLN8 disease 
CLN9 disease 
Congenital neuronal ceroid lipofuscinosis +  
corneal-cerebellar syndrome 
eyelid degenerative disorder +  
FLVCR1-related retinopathy with or without ataxia +  
infantile cerebellar-retinal degeneration 
Krabbe disease +  
Leber hereditary optic neuropathy 
Microphthalmia - brain atrophy 
microphthalmia-brain atrophy syndrome 
Mohr-Tranebjaerg syndrome 
multiple mitochondrial dysfunctions syndrome 4 
muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome 
neuromyelitis optica +   
neuronal ceroid-lipofuscinosis, dominant/recessive 
nystagmus 1, congenital, X-linked 
nystagmus 6, congenital, X-linked 
nystagmus, congenital, autosomal recessive 
osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome 
peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain +  
Progressive epilepsy - intellectual disability, Finnish type 
Refsum disease 
rhizomelic chondrodysplasia punctata type 1 
Sandhoff disease +  
Sjogren-Larsson syndrome 
Spastic paraplegia type 2 
spinocerebellar ataxia 27A 
spinocerebellar ataxia 43 
spinocerebellar ataxia 47 
spinocerebellar ataxia 49 
Spinocerebellar ataxia with axonal neuropathy type 2 
spinocerebellar ataxia, autosomal recessive 24 
Tay-Sachs disease +  
tremor-ataxia-central hypomyelination syndrome 
vitreous syneresis +  
X-linked Charcot-Marie-Tooth disease type 5 
Xeroderma pigmentosum complementation group B 
Xeroderma pigmentosum complementation group D 
Xeroderma pigmentosum complementation group F 
Xeroderma pigmentosum complementation group G 

Synonyms
Exact Synonyms: NYS4 ;   NYSTAGMUS 4, congenital, autosomal dominant
Related Synonyms: vestibulocerebellar disorder with predominant ocular signs
Alternate IDs: MONDO:0008654
Xrefs: MESH:C537856 ;   MIM:193003

paths to the root