Disease #02542 (SCA14 (ataxia, spinocerebellar, type 14 (SCA-14)), OMIM:605361)

Official abbreviation SCA14
Name ataxia, spinocerebellar, type 14 (SCA-14)
OMIM ID 605361
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene PRKCG
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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00073123 - ATX425 - M - France - - - - - SCA14 - PRKCG PRKCG 1 1 Claire Guissart
00073124 - ATX535 - M - France - - - - - SCA14 - PRKCG PRKCG 1 1 Claire Guissart
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
00390050 187548 - - M no Germany - - - - - SCA14 Ataxia, Cerebellar atrophy, Spastic paraplegia, Optic neuropathy, Dysarthria, Difficulty in tongue movements, Hyperreflexia; Son (untested) with similar symptoms PRKCG PRKCG 1 1 Andreas Laner
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