Informaţii despre

Nume Metabolic Acidosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice

Vezi şi

Boli A-Z 3-Methylglutaconic Aciduria 46,xx Sex Reversal 1 Acute Diarrhea Adie Pupil Adult Respiratory Distress Syndrome Aging Albinism Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amblyopia Aniridia 1 Anorexia Nervosa 1 Arterial Calcification, Generalized, of Infancy, 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Asthma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Beriberi Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group--Kidd 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Burns Carcinoid Syndrome Carcinoid Tumors, Intestinal Central Pontine Myelinolysis Cerebritis Cholera Chorioamnionitis Combined Oxidative Phosphorylation Deficiency 12 Congenital Disorder of Glycosylation, Type Iic Cyanide Poisoning Diabetes Mellitus Diarrhea Diarrhea 2, with Microvillus Atrophy Duodenitis Encephalopathy Endotheliitis Enterovesical Fistula Epilepsy Ethylene Glycol Poisoning Fanconi-Bickel Syndrome Fanconi Syndrome Fructose-1,6-Bisphosphatase Deficiency Funisitis Gastroenteritis Gastroschisis Gerstmann-Straussler Disease Glutathione Synthetase Deficiency Gonadal Dysgenesis Hemolytic Anemia Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hepatic Adenomas, Familial Hepatitis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hypoaldosteronism Hypoglycemia Hypokalemia Hypophosphatemia Hyporeninemic Hypoaldosteronism Hypoxia Impaired Renal Function Disease Insulinoma Intracranial Hypertension Ischemia Isolated Optic Neuritis Isoniazid Toxicity Kearns-Sayre Syndrome Kernicterus Lactic Acidosis Laryngitis Leber Congenital Amaurosis Leukodystrophy Leukomalacia Liver Disease Lymphopenia Malaria Medullary Sponge Kidney Meester-Loeys Syndrome Metachromatic Leukodystrophy Methanol Poisoning Methemoglobinemia Migraine with or Without Aura 1 Molybdenum Cofactor Deficiency Monocarboxylate Transporter 1 Deficiency Myasthenia Gravis Myelomeningocele Nephrotic Syndrome Neuronitis Occipital Horn Syndrome Ocular Motor Apraxia Organic Acidemia Overhydrated Hereditary Stomatocytosis Pallister-Hall Syndrome Papillomatosis, Confluent and Reticulated Peritonitis Periventricular Leukomalacia Pitt-Hopkins Syndrome Plasmodium Falciparum Malaria Pneumonia Prader-Willi Syndrome Primary Hyperparathyroidism Propionic Acidemia Pseudohypoaldosteronism Pyloric Stenosis Quadriplegia Rapp-Hodgkin Syndrome Renal Osteodystrophy Renal Tubular Acidosis Renal Tubular Acidosis, Distal Renal Tubular Acidosis, Distal, Autosomal Recessive Renal Tubular Transport Disease Retinitis Short Bowel Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Small Cell Cancer of the Lung Status Asthmaticus Status Epilepticus Thalassemia Thyroiditis Transient Erythroblastopenia of Childhood Tyrosinemia Urea Cycle Disorder Uremia Zygomycosis