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ONTOLOGY REPORT - ANNOTATIONS


Term:hereditary spastic paraplegia 64
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Accession:DOID:0110815 term browser browse the term
Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24. (DO)
Synonyms:exact_synonym: SPG64;   autosomal recessive spastic paraplegia 64;   autosomal recessive spastic paraplegia type 64
 primary_id: OMIM:615683
 alt_id: RDO:9000756
 xref: ORDO:401810
For additional species annotation, visit the Alliance of Genome Resources.


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hereditary spastic paraplegia 64 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 JBrowse link 1 259,692,020 259,818,922 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16017
    disease of anatomical entity 15271
      nervous system disease 10767
        central nervous system disease 8858
          paraplegia 143
            hereditary spastic paraplegia 131
              hereditary spastic paraplegia 64 1
Path 2
Term Annotations click to browse term
  disease 16017
    disease of anatomical entity 15271
      nervous system disease 10767
        central nervous system disease 8858
          neurodegenerative disease 3144
            Nervous System Heredodegenerative Disorders 1897
              motor peripheral neuropathy 521
                hereditary spastic paraplegia 131
                  hereditary spastic paraplegia 64 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.