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ONTOLOGY REPORT - ANNOTATIONS


Term:frontotemporal dementia and/or amyotrophic lateral sclerosis-3
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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: FTDALS3
 primary_id: OMIM:616437
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frontotemporal dementia and/or amyotrophic lateral sclerosis-3 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
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16022
    Developmental Diseases 9336
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8164
        genetic disease 7688
          frontotemporal dementia and/or amyotrophic lateral sclerosis-3 1
Path 2
Term Annotations click to browse term
  disease 16022
    disease of anatomical entity 15275
      nervous system disease 10770
        central nervous system disease 8860
          brain disease 8147
            disease of mental health 5775
              cognitive disorder 1897
                dementia 664
                  Frontotemporal Lobar Degeneration 59
                    frontotemporal dementia 54
                      Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7
                        frontotemporal dementia and/or amyotrophic lateral sclerosis-3 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.