OBO ID: DOID:0050982
Term Name: spinocerebellar ataxia type 35 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by a slowly progressive ataxia, tremor, dysarthria and hyperreflexia, has_material_basis_in mutation in the TGM6 gene. https://www.omim.org/entry/613908
References:
Ontology: Human Disease   ( DOID:0050982 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 35 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TGM6 Spinocerebellar ataxia 35
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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