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Hypophosphatemia
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Acute Leukemia
Acute Liver Failure
Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)
Acute Myocardial Infarction
Acute Pancreatitis
Aging
Al-Raqad Syndrome
Alzheimer Disease 3
Anauxetic Dysplasia 1
Aniridia 1
Ankylosis
Anorexia Nervosa 1
Arterial Calcification of Infancy
Arthrochalasia Ehlers-Danlos Syndrome
Arthrogryposis, Renal Dysfunction, and Cholestasis 1
Asthma
Autism
Autosomal Dominant Polycystic Kidney Disease
Autosomal Recessive Hypophosphatemic Rickets
Autosomal Recessive Non-Syndromic Intellectual Disability
Axial Osteomalacia
Biliary Atresia
Bleeding Disorder, Platelet-Type, 11
Blood Group--Ahonen
Bone Mineral Density Quantitative Trait Locus 15
Bone Mineral Density Quantitative Trait Locus 8
Bone Remodeling Disease
Brittle Bone Disorder
Burns
Calcinosis
Calciphylaxis
Cardiac Arrest
Cardiac Arrhythmia
Cardiogenic Shock
Central Pontine Myelinolysis
Cohen-Gibson Syndrome
Compartment Syndrome
Cutaneous-Skeletal Hypophosphatemia Syndrome
Dental Fluorosis
Dentin Dysplasia
Dentin Dysplasia, Type Ii
Dentinogenesis Imperfecta
Dentinogenesis Imperfecta 1
Diabetes Mellitus
Diarrhea
Dwarfism
Encephalopathy
Enthesopathy
Ethylene Glycol Poisoning
Exfoliation Syndrome
Extraskeletal Chondroma
Familial Tumoral Calcinosis
Fanconi Syndrome
Fibrous Dysplasia
Head Injury
Hemoglobinemia
Hemolytic Anemia
Hemolytic-Uremic Syndrome
Hepatic Adenomas, Familial
Hepatitis
Hepatitis B
Hepatitis C
Hepatitis C Virus
Hepatocellular Carcinoma
Hereditary Hypophosphatemic Rickets
Human Coronavirus Sensitivity
Hypercalciuria, Absorptive, 2
Hyperglycemia
Hyperparathyroidism
Hyperphosphatemia
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
Hypervitaminosis D
Hypoglycemia
Hypokalemia
Hypoparathyroidism
Hypophosphatasia
Hypophosphatasia, Adult
Hypophosphatemic Bone Disease
Hypophosphatemic Rickets, Autosomal Dominant
Hypophosphatemic Rickets with Hypercalciuria, Hereditary
Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Recessive
Idiopathic Hypercalciuria
Impaired Renal Function Disease
Inappropriate Adh Syndrome
Inflammatory Bowel Disease
Influenza
Lactic Acidosis
Legionnaire Disease
Legionnaires' Disease
Leukemia
Liddle Syndrome
Liver Cirrhosis
Lupus Erythematosus
Lymphoblastic Leukemia
Lymphoma
Macroglobulinemia
Macrophage Activation Syndrome
Malaria
Marfan Syndrome
Mccune-Albright Syndrome
Meningitis
Metabolic Acidosis
Mineral Metabolism Disease
Mitochondrial Myopathy
Monoclonal Paraproteinemia
Myeloid Leukemia
Myeloma, Multiple
Myocardial Infarction
Myopathy
Nephrocalcinosis
Nephrolithiasis
Nephrolithiasis/osteoporosis, Hypophosphatemic, 1
Nephrolithiasis, X-Linked Recessive, with Renal Failure
Neuroblastoma
Neuroleptic Malignant Syndrome
Neuropathy
Obstructive Jaundice
Occipital Horn Syndrome
Oncogenic Osteomalacia
Opsismodysplasia
Osteitis Fibrosa
Osteomalacia
Osteopetrosis
Overhydrated Hereditary Stomatocytosis
Pancreatitis
Panic Disorder
Panostotic Fibrous Dysplasia
Paraplegia
Parathyroid Gland Disease
Pericarditis
Periodontitis
Peritonitis
Phosphorus Metabolism Disease
Pitt-Hopkins Syndrome
Pneumonia
Polycystic Kidney Disease
Postural Hypotension
Primary Hyperparathyroidism
Prostate Cancer
Prostatitis
Pseudohypoparathyroidism, Type Ib
Pulmonary Alveolar Microlithiasis
Pulmonary Disease, Chronic Obstructive
Q Fever
Raine Syndrome
Renal Hypodysplasia/aplasia 1
Renal Osteodystrophy
Renal Tubular Acidosis
Rickets
Secondary Hyperparathyroidism of Renal Origin
Sudden Infant Death Syndrome
Systemic Lupus Erythematosus
Three M Syndrome 1
Thrombocytopenia
Thymoma
Thyrotoxic Periodic Paralysis
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