Disease #02634 (SCA17 (ataxia, spinocerebellar, type 17 (SCA-17)), OMIM:607136)

Official abbreviation SCA17
Name ataxia, spinocerebellar, type 17 (SCA-17)
OMIM ID 607136
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene TBP
Associated tissues -
Disease features -
Remarks -


Individuals

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00106553 606181126 - Mother is also affected F ? (Germany) - - - no - SCA1, SCA10, SCA11, SCA14, SCA17, SCA27, SCA5, SCA6, SCA7, SCA8 - FGF14, PRKACG, PRKCG, SPTBN2, TTBK2 PRKCG 1 1 Friederike Hein
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