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

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Official abbreviation	SCA-35
Name	ataxia, spinocerebellar, type 35 (SCA-35)
OMIM ID	613908
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TGM6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-02 11:35:03 +02:00 (CEST)
Date last edited	N/A