Informaţii despre

Nume Lactic Acidosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice; Boli rare
Clasificari ICD10 Acidosis
Boli din aceeaşi familie Lactic Acidosis Congenital Infantile; Lactic Acidosis, Chronic Adult Form

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 3-Methylglutaconic Aciduria Acquired Metabolic Disease Acute Leukemia Acute Liver Failure Acute Myocardial Infarction Acute Pancreatitis Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Ketoglutarate Dehydrogenase Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Aminoaciduria Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Asthma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autoimmune Lymphoproliferative Syndrome, Type V B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas Beriberi Biotinidase Deficiency Biotin-Thiamine-Responsive Basal Ganglia Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I 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 Bowen-Conradi Syndrome Burns Cardiac Arrest Cardiac Tamponade Cardiogenic Shock Cataract Cerebral Hypoxia Cerebritis Cholestasis Chronic Fatigue Syndrome Cocaine Intoxication Coffin-Lowry Syndrome Combined Oxidative Phosphorylation Deficiency 9 Compartment Syndrome Congenital Human Immunodeficiency Virus Cortical Blindness Cranial Nerve Disease Craniosynostosis with Fibular Aplasia Crohn's Colitis Crohn's Disease Cyanide Poisoning Cystic Angiomatosis of Bone, Diffuse Dementia Diabetes Mellitus Diarrhea Diffuse Large B-Cell Lymphoma Ehrlichiosis Encephalitis Encephalomyopathy Encephalopathy Endotheliitis Epilepsy Ethylene Glycol Poisoning Exocrine Pancreatic Insufficiency Fabry Disease Fanconi Syndrome Focal Segmental Glomerulosclerosis Gerstmann-Straussler Disease Glycogen Storage Disease Granulocytopenia Growth Hormone Deficiency Hemoglobinuria Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Herpes Simplex Herpes Simplex Encephalitis Histiocytosis Histoplasmosis Holocarboxylase Synthetase Deficiency Human Immunodeficiency Virus Type 1 Hyperglycemia Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypoaldosteronism Hypoglycemia Hypophosphatemia Hypopituitarism Hyporeninemic Hypoaldosteronism Hypotonia Hypoxia Inherited Metabolic Disorder Interstitial Nephritis Intestinal Pseudo-Obstruction Ischemia Islet Cell Tumor Isoniazid Toxicity Kearns-Sayre Syndrome Kid Syndrome L-2-Hydroxyglutaric Aciduria Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome Leukemia Lung Cancer Lung Disease Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoma Malaria Malignant Histiocytosis Mantle Cell Lymphoma Maple Syrup Urine Disease Melanoma Meningeal Melanoma Meningitis Meningoencephalitis Metabolic Acidosis Mitochondrial Complex I Deficiency Mitochondrial Complex Iii Deficiency Mitochondrial Complex Iv Deficiency Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 9 Mitochondrial Encephalomyopathy Mitochondrial Metabolism Disease Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Myopathy with Lactic Acidosis Monocarboxylate Transporter 1 Deficiency Monocytic Leukemia Mucositis Multidrug-Resistant Tuberculosis Multiple Carboxylase Deficiency Myeloma, Multiple Myocardial Infarction Myoclonic Epilepsy Associated with Ragged-Red Fibers Myoclonus Myoclonus Epilepsy Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2 Myositis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Neuronitis Neuropathy Ocular Motor Apraxia Optic Nerve Disease Optic Nerve Hypoplasia, Bilateral Organic Acidemia Ovarian Hyperstimulation Syndrome Pallister-Hall Syndrome Pancreatitis Pancytopenia Paraneoplastic Syndromes Parkinson Disease 6, Autosomal Recessive Early-Onset Paroxysmal Nocturnal Hemoglobinuria Peritonitis Pernicious Anemia Peroxisome Disorders Pertussis Pfeiffer Syndrome Phaeochromocytoma Pitt-Hopkins Syndrome Plasmablastic Lymphoma Polyneuropathy Prostate Cancer Prostatitis Pulmonary Embolism Pulmonary Hypertension Pyruvate Carboxylase Deficiency Pyruvate Dehydrogenase E1-Alpha Deficiency Pyruvate Dehydrogenase E3-Binding Protein Deficiency Pyruvate Dehydrogenase Phosphatase Deficiency Retinal Detachment Retinitis Sensorineural Hearing Loss Serotonin Syndrome Short Bowel Syndrome Sideroblastic Anemia Small Cell Carcinoma Status Asthmaticus Status Epilepticus Succinic Acidemia Superior Mesenteric Artery Syndrome Thyroid Crisis Thyroiditis Tyrosinemia Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Wolff-Parkinson-White Syndrome