Myopathy, Lactic Acidosis, And Sideroblastic Anemia,Zellweger Syndrome,Myopathy,Optic Nerve Disease,Scotoma,Cockayne Syndrome A,Alzheimer Disease,Mitochondrial Myopathy,Paroxysmal Dystonia,Hereditary Spastic Paraplegia,Skin Amelanotic Melanoma,Autosomal Recessive Spastic Ataxia,Optic Atrophy 1,Brain Cancer,Obesity Due To Melanocortin 4 Receptor Deficiency,Spastic Paraplegia 8,Charcot-Marie-Tooth Disease,Cranial Nerve Disease,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Microcephaly,Encephalopathy,Tooth Disease,Myopathy, Lactic Acidosis, And Sideroblastic Anemia 2,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Lactic Acidosis,Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy,Spinocerebellar Ataxia 12,Optic Atrophy 5,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,Spastic Ataxia,Leigh Syndrome,3-Methylglutaconic Aciduria, Type Iii

Cowpox,Lichen Planus,Hepatitis C,Viral Hepatitis,Viral Encephalitis,Viral Infectious Disease,Hepatitis B,Stomatitis,Dengue Hemorrhagic Fever,Hemorrhagic Disease,Crimean-Congo Hemorrhagic Fever,Pediatric Systemic Lupus Erythematosus,Pityriasis Lichenoides,Relapsing-Remitting Multiple Sclerosis,Influenza,Human Immunodeficiency Virus Infectious Disease,Mumps,Rift Valley Fever,Severe Acute Respiratory Syndrome,Pediculus Humanus Corporis Infestation,Bacterial Infectious Disease,Acute Generalized Exanthematous Pustulosis,Biliary Atresia,Lupus Erythematosus,Childhood Type Dermatomyositis,Rabies,Hantavirus Hemorrhagic Fever With Renal Syndrome,Skin Disease,Multiple Sclerosis,Cutaneous Lupus Erythematosus,Mouth Disease,Swine Influenza,Aicardi-Goutieres Syndrome,Primary Progressive Multiple Sclerosis,Systemic Lupus Erythematosus,Microphthalmia With Limb Anomalies,Subacute Sclerosing Panencephalitis

Influenza,Pediculus Humanus Corporis Infestation,Hantavirus Hemorrhagic Fever With Renal Syndrome,Danubian Endemic Familial Nephropathy,Aicardi-Goutieres Syndrome,Microphthalmia With Limb Anomalies

Zellweger Syndrome,Seizure Disorder,Optic Nerve Disease,Cohen Syndrome,Myopathy, Centronuclear, 1,Undetermined Early-Onset Epileptic Encephalopathy,Peroxisome Biogenesis Disorder 1b,Optic Atrophy 1,Charcot-Marie-Tooth Disease,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 2,Neuronal Intranuclear Inclusion Disease,Centronuclear Myopathy,Disease Of Mental Health,Neuropathy, Hereditary Sensory, Type Id,Aceruloplasminemia,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Lennox-Gastaut Syndrome,Early Infantile Epileptic Encephalopathy,Charcot-Marie-Tooth Disease, Dominant Intermediate B,Developmental And Epileptic Encephalopathy 31,Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive,Rett Syndrome

Myopathy, Centronuclear, 1,Sezary'S Disease,Centronuclear Myopathy,Neuropathy, Hereditary Sensory, Type Id