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MIM:616732 - OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES; OPA10
Xenbase Genes: rtn4ip1
Human Disease Resource: MIM
MONDO:0020737 - optic atrophy 10 with or without ataxia, intellectual disability, and seizures |
DOID:0111434 - optic atrophy 10 |