ONTOLOGY REPORT - ANNOTATIONS


Term:Behr Syndrome
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Accession:DOID:9002421 term browser browse the term
Synonyms:exact_synonym: BEHRS;   infantile hereditary optic atrophy, Behr complicated form of;   infantile hereditary optic atrophy, with neurologic abnormalities
 primary_id: MESH:C537669
 alt_id: OMIM:210000;   RDO:0003549
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Behr Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Opa1 OPA1, mitochondrial dynamin like GTPase JBrowse link 11 74,717,600 74,793,902 RGD:8554872
RGD:7240710

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Path 1
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  disease 14823
    syndrome 4218
      Behr Syndrome 1
Path 2
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  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        central nervous system disease 6908
          brain disease 6412
            disease of mental health 4323
              developmental disorder of mental health 2594
                specific developmental disorder 1329
                  intellectual disability 1157
                    Behr Syndrome 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.