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ONTOLOGY REPORT - ANNOTATIONS


Term:frontotemporal dementia and/or amyotrophic lateral sclerosis-4
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Accession:DOID:0110069 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: FTDALS4
 primary_id: OMIM:616439
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frontotemporal dementia and/or amyotrophic lateral sclerosis-4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kif5a kinesin family member 5A JBrowse link 7 70,515,832 70,552,897 RGD:8554872
G Tbk1 TANK-binding kinase 1 JBrowse link 7 63,655,247 63,687,978 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15984
    Developmental Diseases 9281
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8095
        genetic disease 7613
          frontotemporal dementia and/or amyotrophic lateral sclerosis-4 2
Path 2
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      nervous system disease 10752
        central nervous system disease 8839
          brain disease 8128
            disease of mental health 5761
              cognitive disorder 1895
                dementia 663
                  Frontotemporal Lobar Degeneration 57
                    frontotemporal dementia 52
                      Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 5
                        frontotemporal dementia and/or amyotrophic lateral sclerosis-4 2
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.