Disease #00216 (SCA35 (ataxia, spinocerebellar, type 35 (SCA-35)), OMIM:613908)

Official abbreviation SCA35
Name ataxia, spinocerebellar, type 35 (SCA-35)
OMIM ID 613908
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TGM6
Associated tissues -
Disease features -
Remarks -
Date created 2013-10-02 11:35:03 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00003016 Pat8mov PubMed: Neveling 2013 - - - - - - - - - SCA35 HSP + Ataxia TGM6 TGM6 1 1 Marcel Nelen
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