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optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description A neurologic disorder characterized most commonly by an insidious onset of visual loss and sensorineural hearing loss in childhood with variable presentation of other clinical manifestations including progressive external ophthalmoplegia, muscle cramps, hyperreflexia, and ataxia. There appears to be a wide range of intermediate phenotypes.
Mondo Term and Equivalent IDs
MONDO:0007429:  optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
GARD:0009897: 
UMLS:C3276549: