OBO ID: DOID:0050996
Term Name: episodic ataxia type 8 Search Ontology:
Synonyms:
Definition: An episodic ataxia that is characterized by weakness, dysarthria and myokymia, and has_material_basis_in autosomal dominant inheritance of mutation in the UBR4 gene. https://www.omim.org/entry/616055
References:
Ontology: Human Disease   ( DOID:0050996 )
Relationships
is a type of:
OTHER episodic ataxia type 8 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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