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Nume Hypercalciuria, Absorptive, 2
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Boli din aceeaşi familie Hypercalciuria, Absorptive, 1

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Boli A-Z Acromegaly Adenoma Aging Al-Raqad Syndrome Amelogenesis Imperfecta Aniridia 1 Anorexia Nervosa 1 Antenatal Bartter Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Bartter Disease Bartter Syndrome, Type 2, Antenatal Beckwith-Wiedemann Syndrome Blood Group--Ahonen Blood Group, I System Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brittle Bone Disorder Calciphylaxis Childhood Leukemia Chondrocalcinosis Cohen-Gibson Syndrome Costello Syndrome Cystic Fibrosis Cystinosis Cystinuria Dent Disease 1 Down Syndrome Fanconi-Bickel Syndrome Fanconi Syndrome Gitelman Syndrome Hepatic Adenomas, Familial Hereditary Hypophosphatemic Rickets Hereditary Xanthinuria Horseshoe Kidney Hypercalcemia, Infantile, 1 Hypercalciuria, Absorptive, 1 Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypocalcemia, Autosomal Dominant 1 Hypokalemia Hypomagnesemia 3, Renal Hypoparathyroidism Hypophosphatasia Hypophosphatemia Hypophosphatemic Rickets with Hypercalciuria, Hereditary Hypophosphatemic Rickets, X-Linked Dominant Hypophosphatemic Rickets, X-Linked Recessive Hypouricemia, Renal, 1 Idiopathic Hypercalciuria Juvenile Rheumatoid Arthritis Leukemia Medullary Sponge Kidney Membranous Nephropathy Metabolic Acidosis Mineral Metabolism Disease Myopia Nephrocalcinosis Nephrolithiasis Nephrolithiasis, Calcium Oxalate Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrotic Syndrome Neurofibromatosis, Type Iv, of Riccardi Osteogenesis Imperfecta, Type I Osteomalacia Parathyroid Adenoma Parathyroid Gland Disease Peeling Skin Syndrome Peeling Skin Syndrome 2 Phosphorus Metabolism Disease Primary Fanconi Syndrome Primary Hyperparathyroidism Primary Hypomagnesemia Pseudohypoaldosteronism Pseudohypoaldosteronism, Type Iie Renal Osteodystrophy Renal Tubular Acidosis Renal Tubular Transport Disease Rheumatoid Arthritis Rickets Root Resorption Sarcoidosis 2 Secondary Hyperparathyroidism of Renal Origin Slipped Capital Femoral Epiphysis Thalassemia Wilson Disease Xanthinuria Xanthinuria, Type I