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Metabolic Acidosis
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
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