Term:MAST syndrome
go back to main search page
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.

show annotations for term's descendants       view all columns           Sort by:
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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    syndrome 4220
      MAST syndrome 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
          brain disease 6418
            disease of mental health 4325
              cognitive disorder 1891
                dementia 606
                  MAST syndrome 1
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.