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ONTOLOGY REPORT - ANNOTATIONS


Term:Friedreich ataxia 2
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Accession:DOID:0111219 term browser browse the term
Definition:A Friedreich ataxia that has_material_basis_in mutation in the 9p23-p11 chromosome region. (DO)
Synonyms:exact_synonym: FRDA2
 primary_id: MESH:C566594
 alt_id: DOID:9003073;   OMIM:601992;   RDO:0014907
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Path 1
Term Annotations click to browse term
  disease 15503
    Nutritional and Metabolic Diseases 4395
      disease of metabolism 4395
        mitochondrial metabolism disease 314
          Friedreich ataxia 2
            Friedreich ataxia 2 0
Path 2
Term Annotations click to browse term
  disease 15503
    disease of anatomical entity 14857
      nervous system disease 10273
        central nervous system disease 8410
          brain disease 7763
            movement disease 1010
              Dyskinesias 717
                Ataxia 309
                  hereditary ataxia 191
                    cerebellar ataxia 174
                      autosomal recessive cerebellar ataxia 64
                        Friedreich ataxia 2
                          Friedreich ataxia 2 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.