Mitochondrial Complex I Deficiency

Nume		Mitochondrial Complex I Deficiency
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli genetice; Boli metabolice; Boli rare

Boli A-Z		3-Hydroxyacyl-Coa Dehydrogenase Deficiency Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Atrial Standstill 1 Blood Group--Ahonen Blood Group, I System Brain Small Vessel Disease with or Without Ocular Anomalies Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Axonal, Type 2k Charcot-Marie-Tooth Disease Type 2k Dementia Encephalomyopathy Encephalopathy Epilepsy Fanconi Syndrome Hepatitis Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Lactic Acidosis Lateral Sclerosis Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome Leigh Syndrome with Leukodystrophy Leukodystrophy Liver Disease Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 9 Mitochondrial Encephalomyopathy Mitochondrial Metabolism Disease Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Myoclonic Epilepsy Associated with Ragged-Red Fibers Myopathy Neurofibromatosis, Type Iv, of Riccardi Neuropathy Optic Nerve Disease Optic Nerve Hypoplasia, Bilateral Parkinson Disease 6, Autosomal Recessive Early-Onset Parkinson Disease, Mitochondrial Retinitis Rickets Temporal Lobe Epilepsy Tooth Disease