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ONTOLOGY REPORT - ANNOTATIONS


Term:MAST syndrome
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Accession:DOID:0060245 term browser browse the term
Definition:A hereditary spastic paraplegia associated with dementia. (DO)
Synonyms:exact_synonym: SPG21;   Spastic Paraplegia 21, Autosomal Recessive;   autosomal recessive spastic paraplegia type 21;   hereditary spastic paraplegia 21
 primary_id: MESH:C565409;   RDO:0014052
 alt_id: OMIM:248900
 xref: ORDO:101001
For additional species annotation, visit the Alliance of Genome Resources.


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MAST syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Spg21 SPG21 abhydrolase domain containing, maspardin JBrowse link 8 70,994,531 71,022,302 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16022
    syndrome 6143
      MAST syndrome 1
Path 2
Term Annotations click to browse term
  disease 16022
    disease of anatomical entity 15275
      nervous system disease 10770
        central nervous system disease 8860
          brain disease 8147
            disease of mental health 5775
              cognitive disorder 1897
                dementia 664
                  MAST syndrome 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.