Informaţii despre

Nume Leigh Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Other specified degenerative diseases of nervous system
Clasificare anatomică Malacards Boli ale ochiului; Boli cardiovasculare; Boli neuronale

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 3-Methylglutaconic Aciduria 3-Methylglutaconic Aciduria, Type Iv 3-Methylglutaconic Aciduria, Type V 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome Aceruloplasminemia Acquired Idiopathic Sideroblastic Anemia Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Alzheimer Disease Mitochondrial Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Atrial Standstill 1 Basal Ganglia Disease Biotinidase Deficiency Biotin-Thiamine-Responsive Basal Ganglia Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brain Injury Cardioencephalomyopathy Carney Triad Cataract Central Nervous System Vasculitis Cercarial Dermatitis Chronic Progressive External Ophthalmoplegia Coenzyme Q10 Deficiency Disease Congenital Muscular Dystrophy Type 1a Coq-Responsive Oxphos Deficiency Cortical Blindness Cowden Syndrome 3 Craniosynostosis 1 Diabetes and Deafness, Maternally Inherited Diphyllobothriasis Dysphagia Dystonia Echinococcosis Encephalomyopathy Encephalopathy Epilepsy Fatal Infantile Cytochrome C Oxidase Deficiency Fatal Infantile Encephalocardiomyopathy Fontaine Progeroid Syndrome Genetic Recurrent Myoglobinuria Growth Hormone Deficiency Hepatic Adenomas, Familial Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypertrophic Olivary Degeneration Hypotonia Hypoxia Infantile Apnea Kearns-Sayre Syndrome Lactic Acidosis Laryngeal Cleft Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome, French Canadian Type Leigh Syndrome with Leukodystrophy Leigh Syndrome with Nephrotic Syndrome Leukodystrophy Leukoencephalopathy, Hereditary Diffuse, with Spheroids Mitochondrial Complex I Deficiency Mitochondrial Complex Ii Deficiency Mitochondrial Complex Iii Deficiency Mitochondrial Complex Iv Deficiency Mitochondrial Complex V Deficiency Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 1 Mitochondrial Encephalomyopathy Mitochondrial Metabolism Disease Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mohr-Tranebjaerg Syndrome Muir-Torre Syndrome Muscular Dystrophy Myoclonic Epilepsy Associated with Ragged-Red Fibers Myoclonus Myopathy Necrotizing Encephalomyelopathy, Subacute, of Leigh, Adult Neural Crest Tumor Neuronitis Neuropathy Neuropathy, Hereditary Motor and Sensory, Type Via Nonsyndromic Deafness Nuclear Gene-Encoded Leigh Syndrome Optic Nerve Disease Orbit Rhabdomyosarcoma Paraganglioma and Gastric Stromal Sarcoma Paragangliomas 1 Placental Site Trophoblastic Tumor Ptosis Pyruvate Dehydrogenase E1-Alpha Deficiency Pyruvate Dehydrogenase E3-Binding Protein Deficiency Rhabdomyosarcoma Schizophrenia Sparganosis Spasticity Sulfite Oxidase Deficiency, Isolated Tetraamelia Syndrome, Autosomal Recessive Traumatic Brain Injury Vasculitis West Syndrome Wolff-Parkinson-White Syndrome