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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
episodic ataxia +     
episodic ataxia type 1  
episodic ataxia type 2  
episodic ataxia type 3 
episodic ataxia type 4 
episodic ataxia type 5  
episodic ataxia type 6  
episodic ataxia type 7 
episodic ataxia type 8 
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. (DO)
Episodic Ataxia Type 9  
Intellectual Disability with Episodic Ataxia and Congenital Arthrogryposis  

Synonyms
Primary IDs: OMIM:616055
Definition Sources: https://www.omim.org/entry/616055 "DO" "DO"

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