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syndromic genetic deafness
?
TBD
human disease
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Subclasses
5
MELAS syndrome
Mitochondrial disease
Autosomal dominant cerebellar ataxia, deafness, and narcolepsy
Medical condition
combined oxidative phosphorylation defect type 25
human disease
Norrie disease
Genetic disorder that primarily affects the eye
Kearns–Sayre syndrome
Genetic mitochondrial disease
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Instance of
head and neck disease
developmental defect during embryogenesis
class of disease
Subclass of
rare genetic developmental defect during embryogenesis
developmental defect during embryogenesis
Wikidata
