ONTOLOGY REPORT - ANNOTATIONS


Term:hereditary spastic paraplegia 73
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Accession:DOID:0110818 term browser browse the term
Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the CPT1C gene on chromosome 19q13. (DO)
Synonyms:exact_synonym: SPG73;   autosomal dominant spastic paraplegia 73;   autosomal dominant spastic paraplegia type 73
 primary_id: OMIM:616282
 alt_id: RDO:9001558
 xref: ORDO:444099
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hereditary spastic paraplegia 73 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cpt1c carnitine palmitoyltransferase 1c JBrowse link 1 100,955,094 100,970,579 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        central nervous system disease 6913
          paraplegia 134
            hereditary spastic paraplegia 120
              hereditary spastic paraplegia 73 1
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        central nervous system disease 6913
          neurodegenerative disease 2092
            Nervous System Heredodegenerative Disorders 1168
              motor peripheral neuropathy 413
                hereditary spastic paraplegia 120
                  hereditary spastic paraplegia 73 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.