Syndrome hypophosphatemia or hypophosphatemic rickets. Medical search. Frequent questions

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Anatomy5

Osteocytes X Chromosome Kidney Dental Cementum Bone and Bones

Diseases23

Familial Hypophosphatemic Rickets Hypophosphatemia Hypophosphatemia, Familial Rickets Genetic Diseases, X-Linked Osteomalacia Hypercalciuria Nephrocalcinosis Rickets, Hypophosphatemic Nevus, Sebaceous of Jadassohn Tooth Mobility Fanconi Syndrome Dentin Dysplasia Syndrome Hyperparathyroidism Nephrolithiasis Neoplasms, Connective Tissue Hyperphosphatemia Hypocalcemia Refeeding Syndrome Paraneoplastic Syndromes Mesenchymoma Vitamin D Deficiency

Chemicals and Drugs20

PHEX Phosphate Regulating Neutral Endopeptidase Sodium-Phosphate Cotransporter Proteins, Type IIc Phosphates Fibroblast Growth Factors Sodium-Phosphate Cotransporter Proteins, Type IIa Phosphorus Calcitriol Parathyroid Hormone Hydroxycholecalciferols Extracellular Matrix Proteins Sodium-Phosphate Cotransporter Proteins Pyrophosphatases 25-Hydroxyvitamin D3 1-alpha-Hydroxylase Vitamin D Phosphoric Diester Hydrolases Glucuronidase Sodium-Phosphate Cotransporter Proteins, Type I Phosphoproteins Calcium Sodium-Phosphate Cotransporter Proteins, Type II

Analytical, Diagnostic and Therapeutic Techniques and Equipment2

DNA Mutational Analysis Pedigree

Phenomena and Processes8

Calcification, Physiologic Tooth Mobility X Chromosome Mutation Genes, Recessive Mutation, Missense Genetic Linkage Phenotype

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes

Familial Hypophosphatemic Rickets Hypophosphatemia Hypophosphatemia, Familial Rickets PHEX Phosphate Regulating Neutral Endopeptidase Sodium-Phosphate Cotransporter Proteins, Type IIc Genetic Diseases, X-Linked Osteomalacia Hypercalciuria Phosphates Nephrocalcinosis Fibroblast Growth Factors Rickets, Hypophosphatemic Sodium-Phosphate Cotransporter Proteins, Type IIa Phosphorus Calcitriol Nevus, Sebaceous of Jadassohn Calcification, Physiologic Tooth Mobility Fanconi Syndrome Dentin Dysplasia Syndrome Parathyroid Hormone Osteocytes Hydroxycholecalciferols Extracellular Matrix Proteins Hyperparathyroidism X Chromosome Sodium-Phosphate Cotransporter Proteins Mutation Pyrophosphatases Genes, Recessive DNA Mutational Analysis Kidney Nephrolithiasis 25-Hydroxyvitamin D3 1-alpha-Hydroxylase Mutation, Missense Vitamin D Pedigree Genetic Linkage Neoplasms, Connective Tissue Phosphoric Diester Hydrolases Hyperphosphatemia Phenotype Glucuronidase Dental Cementum Hypocalcemia Refeeding Syndrome Bone and Bones Sodium-Phosphate Cotransporter Proteins, Type I Phosphoproteins Paraneoplastic Syndromes Calcium Sodium-Phosphate Cotransporter Proteins, Type II Mesenchymoma Vitamin D Deficiency

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