ONTOLOGY REPORT - ANNOTATIONS


Term:hereditary spastic paraplegia 9B
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Accession:DOID:0110825 term browser browse the term
Definition:A neurologic disorder characterized by early-onset complex spastic paraplegia. Affected individuals had delayed psychomotor development, intellectual disability, and severe motor impairment. (OMIM)
Synonyms:exact_synonym: SPG9B;   autosomal recessive complex spastic paraplegia type 9B;   autosomal recessive spastic paraplegia 9B
 primary_id: OMIM:616586
 alt_id: RDO:9001562
 xref: ORDO:447760
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hereditary spastic paraplegia 9B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Aldh18a1 aldehyde dehydrogenase 18 family, member A1 JBrowse link 1 259,641,673 259,674,521 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        central nervous system disease 6908
          paraplegia 134
            hereditary spastic paraplegia 120
              hereditary spastic paraplegia 9B 1
Path 2
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        central nervous system disease 6908
          neurodegenerative disease 2091
            Nervous System Heredodegenerative Disorders 1168
              motor peripheral neuropathy 413
                hereditary spastic paraplegia 120
                  hereditary spastic paraplegia 9B 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.