OBO ID: DOID:0050993
Term Name: episodic ataxia type 5 Search Ontology:
Synonyms:
Definition: An episodic ataxia that is characterized by dysarthria and vertigo, develops in early childhood, and has_material_basis_in autosomal dominant inheritance of mutation in the CACNB4 gene. https://www.omim.org/entry/613855
References:
Ontology: Human Disease   ( DOID:0050993 )
Relationships
is a type of:
OTHER episodic ataxia type 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CACNB4 Episodic ataxia, type 5 613855
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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