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hereditary spastic paraplegia 37 - Ontology Report - Rat Genome Database

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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:hereditary spastic paraplegia 37
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Accession:DOID:0110788 term browser browse the term
Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3. (DO)
Synonyms:exact_synonym: SPG37;   autosomal dominant spastic paraplegia 37;   autosomal dominant spastic paraplegia type 37
 primary_id: MESH:C567931
 alt_id: MIM:611945;   RDO:0012082
 xref: ORDO:171612

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Path 1
Term Annotations click to browse term
  disease 288179
    disease of anatomical entity 271815
      nervous system disease 190640
        central nervous system disease 157774
          paraplegia 7142
            hereditary spastic paraplegia 4775
              hereditary spastic paraplegia 37 0
Path 2
Term Annotations click to browse term
  disease 288179
    disease of anatomical entity 271815
      nervous system disease 190640
        central nervous system disease 157774
          neurodegenerative disease 56131
            Nervous System Heredodegenerative Disorders 34568
              motor peripheral neuropathy 13240
                hereditary spastic paraplegia 4775
                  hereditary spastic paraplegia 37 0
paths to the root