Mitochondrial Dna Depletion Syndrome,Squamous Cell Carcinoma,Retinitis Pigmentosa,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 1,Myopathy,Mitochondrial Myopathy,Mitochondrial Metabolism Disease,Lung Sarcomatoid Carcinoma,Axonal Neuropathy,Mitochondrial Neurogastrointestinal Encephalomyopathy,Chronic Progressive External Ophthalmoplegia,Mitochondrial Dna Depletion Syndrome 7,Ocular Motility Disease,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 5,Sensorineural Hearing Loss,Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form,Autosomal Dominant Progressive External Ophthalmoplegia,Mitochondrial Disorders,Rrm2b-Related Mitochondrial Disease,Fanconi Syndrome,Camptocormism,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 4,Mitochondrial Dna Depletion Syndrome 4b,Lactic Acidosis,Fanconi Renotubular Syndrome 1,Mitochondrial Dna Depletion Syndrome 8a,Metabolic Acidosis,Cone Dystrophy,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 2,Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis,Leber Hereditary Optic Neuropathy, Modifier Of,Mitochondrial Dna Depletion Syndrome 4a,Ptosis,Kearns-Sayre Syndrome,Leigh Syndrome,Pearson Marrow-Pancreas Syndrome,Deafness, Aminoglycoside-Induced,Mitochondrial Dna Depletion Syndrome 6

Skin Melanoma,Colorectal Cancer,Hepatocellular Carcinoma,Breast Disease,Choriocarcinoma,Diamond-Blackfan Anemia 20,Syndromic X-Linked Intellectual Disability 94,Lung Cancer,Pancreatic Cancer