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ONTOLOGY REPORT - ANNOTATIONS


Term:FTDALS3
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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
For additional species annotation, visit the Alliance of Genome Resources.


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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
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          FTDALS3 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      nervous system disease 9141
        central nervous system disease 6931
          brain disease 6435
            disease of mental health 4324
              cognitive disorder 1834
                dementia 615
                  Frontotemporal Lobar Degeneration 38
                    frontotemporal dementia 32
                      Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4
                        FTDALS3 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.