Disease #02456 (SCA-10 (ataxia, spinocerebellar, type 10 (SCA-10)), OMIM:603516)

Official abbreviation SCA-10
Name ataxia, spinocerebellar, type 10 (SCA-10)
OMIM ID 603516
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 1 gene ATXN10
Associated tissues -
Disease features -
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Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00104046 11017075-FamA PubMed: Matsuura 2000, Journal: Matsuura 2000 3-generation family, 10 affecteds (5F, 5M) F;M no Mexico - - 0 - - SCA-10 cerebellar ataxia, seizures ATXN10 ATXN10 1 10 Johan den Dunnen
00104047 11017075-FamB PubMed: Matsuura 2000, Journal: Matsuura 2000 2-generation family, affected sister/brother F;M no Mexico - - 0 - - SCA-10 cerebellar ataxia, seizures ATXN10 ATXN10 1 2 Johan den Dunnen
00104048 11017075-FamC PubMed: Matsuura 2000, Journal: Matsuura 2000 3-generation family, 9 affecteds (6F, 3M) F;M no Mexico - - 0 - - SCA-10 cerebellar ataxia, seizures - - 0 9 Johan den Dunnen
00106553 606181126 - Mother is also affected F ? (Germany) - - 0 no - SCA-1, SCA-10, SCA-11, SCA-14, SCA-17, SCA-27, SCA-5, SCA-6, SCA-7, SCA-8 - FGF14, PRKACG, PRKCG, SPTBN2, TTBK2 PRKCG 1 1 Friederike Hein
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