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Nume Mitochondrial Disorders
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Boli A-Z 3-Hydroxyisobutyryl-Coa Hydrolase Deficiency 3-Methylglutaconic Aciduria, Type Iii 3-Methylglutaconic Aciduria, Type V Aging Alexander Disease Al-Raqad Syndrome Alzheimer Disease Mitochondrial Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autism Autism Spectrum Disorder Autosomal Dominant Progressive External Ophthalmoplegia Axonal Neuropathy Basal Ganglia Calcification Blood Group--Ahonen Blood Group, Dombrock System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Burns Cardioencephalomyopathy Cardiomyopathy, Infantile Histiocytoid Carrion's Disease Cataract Cercarial Dermatitis Cerebral Creatine Deficiency Syndrome 1 Cerebritis Chronic Fatigue Syndrome Chronic Progressive External Ophthalmoplegia Coenzyme Q10 Deficiency Disease Combined Oxidative Phosphorylation Deficiency 19 Cortical Blindness Cranial Nerve Disease Crouzon Syndrome Cyclic Vomiting Syndrome Deafness, Aminoglycoside-Induced Deafness, Nonsyndromic Sensorineural, Mitochondrial Dementia Diabetes and Deafness, Maternally Inherited Diabetic Polyneuropathy Dilated Cardiomyopathy Diphyllobothriasis Dystrophinopathies Early Myoclonic Encephalopathy Encephalitis Encephalomyopathy Encephalopathy Epilepsy Fanconi Anemia, Complementation Group E Fatal Infantile Cytochrome C Oxidase Deficiency Fatal Infantile Encephalocardiomyopathy Gastroparesis Growth Hormone Deficiency Headache Hepatitis Hereditary Ataxia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypertrophic Olivary Degeneration Hypogonadism Isolated Atp Synthase Deficiency Kearns-Sayre Syndrome Lactic Acidosis Lateral Sclerosis Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome Lipomatosis Liver Disease Malignant Hyperthermia Malignant Hyperthermia Susceptibility Maternally-Inherited Progressive External Ophthalmoplegia Microcephaly Mitochondrial Complex I Deficiency Mitochondrial Complex Iv Deficiency Mitochondrial Complex V Deficiency Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 1 Mitochondrial Dna Depletion Syndrome 3 Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Dna Depletion Syndrome 7 Mitochondrial Encephalomyopathy Mitochondrial Metabolism Disease Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Neurogastrointestinal Encephalomyopathy Mitochondrial Neurogastrointestinal Encephalopathy Disease Mitochondrial Non-Syndromic Sensorineural Deafness Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Sclerosis Multiple Symmetrical Lipomatosis Muscular Dystrophy Myasthenic Syndrome, Congenital, 10 Myoclonic Epilepsy Associated with Ragged-Red Fibers Myoclonus Myoclonus Epilepsy Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia Myotonia Neuronitis Neuropathy Neutropenia Ocular Motility Disease Optic Nerve Disease Parkinson Disease 6, Autosomal Recessive Early-Onset Parkinson Disease, Mitochondrial Pearson Marrow-Pancreas Syndrome Polycystic Ovary Syndrome Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 1 Pulmonary Hypertension Renal Tubular Acidosis Retinitis Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis Sideroblastic Anemia Sparganosis Spasticity Spastic Paraparesis Spastic Paraplegia 7, Autosomal Recessive Spondyloocular Syndrome Stereotypic Movement Disorder Undifferentiated Pleomorphic Sarcoma Vici Syndrome Wolfram Syndrome