Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:616732 - OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES; OPA10


Xenbase Genes: rtn4ip1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0020737 - optic atrophy 10 with or without ataxia, intellectual disability, and seizures

Disease Ontology (DO):
DOID:0111434 - optic atrophy 10