Informaţii despre

Nume Renal Tubular Acidosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Renal Tubular Acidosis Iii

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Boli A-Z Acute Urate Nephropathy Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Amelogenesis Imperfecta Aminoaciduria Aniridia 1 Anorexia Nervosa 1 Apparent Mineralocorticoid Excess Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 3 Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autoimmune Disease Autoimmune Hepatitis Bartter Disease Bartter Syndrome, Type 2, Antenatal Blood Group--Ahonen Blood Group, I System Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Branchiootic Syndrome 1 Carnitine Palmitoyltransferase I Deficiency Cataract Celiac Disease 1 Cerebritis Chilaiditi Syndrome Cholangitis Cholestasis Coffin-Lowry Syndrome Cohen-Gibson Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cutis Laxa Cystinosis Cystinuria Dandy-Walker Syndrome Dental Caries Diabetes Insipidus Diabetes Mellitus Diarrhea 1, Secretory Chloride, Congenital Disseminated Intravascular Coagulation Elliptocytosis 2 Empty Sella Syndrome Encephalopathy Fanconi-Bickel Syndrome Fanconi Renotubular Syndrome 1 Fanconi Syndrome Focal Segmental Glomerulosclerosis Galactorrhea Glioma Glomerulonephritis Glucose/galactose Malabsorption Growth Hormone Deficiency Hashimoto Thyroiditis Hemoglobinopathy Hemolytic Anemia Hepatitis Hereditary Elliptocytosis Hereditary Spherocytosis Hereditary Xanthinuria Hyperaldosteronism, Familial, Type I Hyperparathyroidism Hyperthyroidism Hypoaldosteronism Hypokalemia Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hyporeninemic Hypoaldosteronism Immunoglobulin E Concentration, Serum Infantile Mercury Poisoning Interstitial Nephritis Ischemia Isolated Optic Neuritis Kearns-Sayre Syndrome Leptospirosis Leukemia Leukodystrophy Liddle Syndrome Liver Disease Lowe Oculocerebrorenal Syndrome Lung Cancer Lupus Erythematosus Lymphoid Interstitial Pneumonia Lymphoid Leukemia Lymphoma Lymphoplasmacytic Lymphoma Macroglobulinemia Medullary Sponge Kidney Membranoproliferative Glomerulonephritis Mercury Poisoning Metabolic Acidosis Metachromatic Leukodystrophy Methemoglobinemia Microcytic Anemia Mitochondrial Complex V Deficiency, Nuclear Type 1 Mitochondrial Disorders Myopathy Nephrocalcinosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrotic Syndrome Neuroaxonal Dystrophy Osteomalacia Osteopetrosis Osteopetrosis, Autosomal Recessive 3 Ovalocytosis, Southeast Asian Pitt-Hopkins Syndrome Pneumonia Polymyositis Posterior Urethral Valves Primary Biliary Cirrhosis Primary Fanconi Syndrome Primary Hyperoxaluria Primary Hyperparathyroidism Proteus Syndrome Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Pseudohypoaldosteronism Pseudohypoaldosteronism, Type I, Autosomal Dominant Pseudohypoaldosteronism, Type I, Autosomal Recessive Pseudohypoparathyroidism Purpura Pyruvate Carboxylase Deficiency Renal Dysplasia Renal Tubular Acidosis, Distal Renal Tubular Acidosis, Distal, Autosomal Dominant Renal Tubular Acidosis, Distal, Autosomal Recessive Renal Tubular Acidosis, Proximal Renal Tubular Acidosis, Proximal, with Ocular Abnormalities and Mental Retardation Renal Tubular Transport Disease Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Rett Syndrome Rheumatoid Arthritis Rickets Sclerosing Cholangitis Sensorineural Hearing Loss Silver-Russell Syndrome Sjogren Syndrome Slc4a1-Associated Distal Renal Tubular Acidosis Spastic Ataxia, Charlevoix-Saguenay Type Spastic Diplegia Spasticity Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spondyloocular Syndrome Superior Mesenteric Artery Syndrome Systemic Lupus Erythematosus Thrombosis Thyroiditis Tuberous Sclerosis Urethritis Urinary Tract Obstruction Vasculitis Vici Syndrome Wilms Tumor 6 Xanthinuria