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ONTOLOGY REPORT - ANNOTATIONS


Term:Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy
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Accession:DOID:9005240 term browser browse the term
Definition:An autosomal recessive progressive disorder characterized by onset of gait ataxia, cognitive decline, and gaze palsy in the first or second decades. Additional features include dysarthria, dystonia, and athetoid movements. (OMIM)
Synonyms:exact_synonym: NADGP
 primary_id: OMIM:617145
 alt_id: RDO:9001504
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Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sqstm1 sequestosome 1 JBrowse link 10 35,704,728 35,716,316 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      nervous system disease 10216
        neurodegenerative disease 2691
          Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      nervous system disease 10216
        central nervous system disease 8092
          neurodegenerative disease 2691
            Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy 1
paths to the root

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