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Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.
Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"
Mitochondrial DNA-related cardiomyopathy and hearing loss
mtDNA-related cardiomyopathy and deafness · Maternally-inherited cardiomyopathy and deafness
Dilated cardiomyopathy
Mitochondrial DNA-related mitochondrial myopathy
mtDNA-related mitochondrial myopathy · Maternally-inherited mitochondrial myopathy
Sensorineural deafness with dilated cardiomyopathy
Neurosensory deafness with dilated cardiomyopathy · Neurosensory hearing loss with dilated cardiomyopathy