Disease #02456 (SCA10 (ataxia, spinocerebellar, type 10 (SCA-10)), OMIM:603516)

Official abbreviation SCA10
Name ataxia, spinocerebellar, type 10 (SCA-10)
OMIM ID 603516
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 1 gene ATXN10
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


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 - - - - - SCA10 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 - - - - - SCA10 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 - - - - - SCA10 cerebellar ataxia, seizures - - - 9 Johan den Dunnen
00106553 606181126 - Mother is also affected F ? (Germany) - - - no - SCA1, SCA10, SCA11, SCA14, SCA17, SCA27A, SCA5, SCA6, SCA7, SCA8 - FGF14, PRKACG, PRKCG, SPTBN2, TTBK2 PRKCG 1 1 Friederike Hein
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