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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:spinocerebellar ataxia type 37
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Accession:EFO:MONDO:0014410 term browser browse the term
Definition:Spinocerebellar ataxia type 37 (SCA37) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1), characterized by a cerebellar syndrome along with altered vertical eye movements.
Synonyms:exact_synonym: SCA37;   spinocerebellar ataxia with altered vertical eye movements
 related_synonym: spinocerebellar ataxia 37
 alt_id: MONDO:0014410
 xref: DOID:0050984;   GARD:12368;   MEDGEN:855217;   MIM:615945;   ORDO:363710;   SCTID:719301002;   UMLS:C3889636


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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 37 0
Path 2
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  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 37 0
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