syndromic genetic deafness · human disease · YYNN

syndromic genetic deafness

? TBD

human disease

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Subclasses 5

Influences rating

Mitochondrial disease

Autosomal dominant cerebellar ataxia, deafness, and narcolepsy

Medical condition

combined oxidative phosphorylation defect type 25

Genetic disorder that primarily affects the eye

Kearns–Sayre syndrome

Genetic mitochondrial disease

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