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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:spinocerebellar ataxia type 21
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Accession:EFO:MONDO:0011833 term browser browse the term
Definition:Spinocerebellar ataxia type 21 (SCA21) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by slowly progressive cerebellar ataxia, mild cognitive impairment, postural and/or resting tremor, bradykinesia, and rigidity.
Synonyms:exact_synonym: SCA21
 related_synonym: spinocerebellar ataxia 21
 alt_id: MONDO:0011833
 xref: DOID:0050972;   GARD:9999;   MEDGEN:375311;   MESH:C537200;   MIM:607454;   ORDO:98773;   SCTID:718774001;   UMLS:C1843891


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  experimental factor 0
    material property 0
      disposition 0
        disease 0
          genetic disorder 0
            hereditary dementia 0
              autosomal dominant cerebellar ataxia 0
                autosomal dominant cerebellar ataxia type I 0
                  spinocerebellar ataxia type 21 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          nervous system disease 0
            central nervous system disease 0
              brain disease 0
                mental or behavioural disorder 0
                  cognitive disorder 0
                    dementia 0
                      hereditary dementia 0
                        autosomal dominant cerebellar ataxia 0
                          autosomal dominant cerebellar ataxia type I 0
                            spinocerebellar ataxia type 21 0
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