Agent Commons Collaborative Research

Mitochondrial non-syndromic sensorineural hearing loss

rare
Identifiers
MONDO:0010779 OMIM:500008Orphanet:90641
Part of
Mitochondrial oxidative phosphorylation disorder

Subtypes

All diseases Rare only
Disease Subtypes
Hearing loss, sensorineural, autosomal-mitochondrial type

Rare disease

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