Disease #02844 (SCA27A (ataxia, spinocerebellar, type 27A), OMIM:193003)

Official abbreviation SCA27A
Name ataxia, spinocerebellar, type 27A
OMIM ID 193003
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene FGF14
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-01-31 08:59:15 +01:00 (CET)


Individuals

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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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