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Nume Mitochondrial Metabolism Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 3-Methylglutaconic Aciduria, Type Iii 3-Methylglutaconic Aciduria, Type Iv 3-Methylglutaconic Aciduria, Type V Acute Liver Failure Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Alzheimer Disease Mitochondrial Aniridia 1 Anorexia Nervosa 1 Ataxia and Polyneuropathy, Adult-Onset Autism Autism Spectrum Disorder Autonomic Dysfunction Autosomal Dominant Progressive External Ophthalmoplegia Axonal Neuropathy Behr Syndrome Blood Group--Ahonen Cardioencephalomyopathy Carpal Tunnel Syndrome Cerebral Folate Deficiency Cerebritis Cerebrotendinous Xanthomatosis Charcot-Marie-Tooth Disease Chronic Progressive External Ophthalmoplegia Coenzyme Q10 Deficiency Disease Combined Oxidative Phosphorylation Deficiency Complex Regional Pain Syndrome Congenital Cataract-Hypertrophic Cardiomyopathy-Mitochondrial Myopathy Syndrome Cortical Blindness Cranial Nerve Disease Cyclic Vomiting Syndrome Cystinuria Diabetes and Deafness, Maternally Inherited Diphyllobothriasis Dysphagia Dystonia Dystrophinopathies Encephalomyopathy End Stage Renal Failure Epilepsy Fatal Infantile Cytochrome C Oxidase Deficiency Fatal Infantile Encephalocardiomyopathy Focal Segmental Glomerulosclerosis Growth Hormone Deficiency Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperphenylalaninemia Hypertrichosis Hypertrophic Cardiomyopathy Hypertrophic Olivary Degeneration Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Inherited Metabolic Disorder Intestinal Pseudo-Obstruction Kearns-Sayre Syndrome Lactic Acidosis Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome Leigh Syndrome with Leukodystrophy Malignant Hyperthermia Malignant Hyperthermia Susceptibility Maternally-Inherited Progressive External Ophthalmoplegia Microphthalmia Mitochondrial Complex I Deficiency Mitochondrial Complex Iv Deficiency Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 1 Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Dna Depletion Syndrome 7 Mitochondrial Encephalomyopathy Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Neurogastrointestinal Encephalomyopathy Mononeuropathy of the Median Nerve, Mild Myoclonic Epilepsy Associated with Ragged-Red Fibers Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia Myotonic Dystrophy Neuropathy Ocular Motility Disease Optic Nerve Disease Paine Syndrome Parkinson Disease 6, Autosomal Recessive Early-Onset Pearson Marrow-Pancreas Syndrome Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Ptosis Pulmonary Edema Pyruvate Dehydrogenase E1-Alpha Deficiency Reflex Sympathetic Dystrophy Rrm2b-Related Mitochondrial Disease Sengers Syndrome Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis Sparganosis Spastic Paraplegia 7, Autosomal Recessive Spinocerebellar Atrophy Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Succinate-Coa Ligase Deficiency Tooth Disease Wolfram Syndrome Xanthomatosis