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ONTOLOGY REPORT - ANNOTATIONS


Term:hereditary spastic paraplegia 13
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Accession:DOID:0110766 term browser browse the term
Definition:A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 on chromosome 2q33. (DO)
Synonyms:exact_synonym: SPG13;   autosomal dominant spastic paraplegia 13
 primary_id: MESH:C537485
 alt_id: OMIM:605280;   RDO:0003331
 xref: GARD:9616;   ORDO:100994
For additional species annotation, visit the Alliance of Genome Resources.


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hereditary spastic paraplegia 13 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hspd1 heat shock protein family D (Hsp60) member 1 JBrowse link 9 61,680,529 61,691,202 RGD:7240710
RGD:10402832
RGD:8554872
RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14096
      nervous system disease 9148
        central nervous system disease 6948
          paraplegia 136
            hereditary spastic paraplegia 122
              hereditary spastic paraplegia 13 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14096
      nervous system disease 9148
        central nervous system disease 6948
          neurodegenerative disease 2549
            Nervous System Heredodegenerative Disorders 1620
              motor peripheral neuropathy 416
                hereditary spastic paraplegia 122
                  hereditary spastic paraplegia 13 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.