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syndromic genetic deafness
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MELAS syndrome
?
TBD
Mitochondrial disease
Autosomal dominant cerebellar ataxia, deafness, and narcolepsy
?
TBD
Medical condition
combined oxidative phosphorylation defect type 25
?
TBD
human disease
Norrie disease
?
TBD
Genetic disorder that primarily affects the eye
Kearns–Sayre syndrome
?
TBD
Genetic mitochondrial disease
