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Accession:DOID:0110068 term browser browse the term
Definition: An autosomal dominant neurodegenerative disorder characterized by adult or late adult onset of cognitive impairment, behavioral abnormalities, and speech apraxia and/or upper and lower motor neuron signs.(OMIM)
Synonyms:exact_synonym: frontotemporal dementia and/or amyotrophic lateral sclerosis 3
 primary_id: OMIM:616437;   RDO:9000424
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FTDALS3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sqstm1 sequestosome 1 JBrowse link 10 35,704,728 35,716,316 RGD:7240710

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Path 1
Term Annotations click to browse term
  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          FTDALS3 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        central nervous system disease 6892
          brain disease 6396
            disease of mental health 4314
              cognitive disorder 1888
                dementia 603
                  Frontotemporal Lobar Degeneration 39
                    frontotemporal dementia 33
                      FTDALS3 1
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