Informaţii despre

Nume Hypophosphatemic Rickets, X-Linked Recessive
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificare anatomică Malacards Boli endocrine; Boli nefrologice (ale rinichilor); Boli osoase

Vezi şi

Boli A-Z Aggressive Periodontitis Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aminoaciduria Aniridia 1 Anorexia Nervosa 1 Arterial Calcification of Infancy Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autosomal Recessive Hypophosphatemic Rickets Blood Group--Ahonen Blood Group, Dombrock System Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bone Remodeling Disease Brittle Bone Disorder Calcinosis Calciphylaxis Central Precocious Puberty Cervicitis Craniosynostosis Dental Abscess Dent Disease 1 Dentin Dysplasia Dentin Dysplasia, Type Ii Dentinogenesis Imperfecta Dentinogenesis Imperfecta 1 Enthesopathy Exfoliation Syndrome Familial Glucocorticoid Deficiency Familial Tumoral Calcinosis Fanconi-Bickel Syndrome Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fibrous Dysplasia Giant Congenital Nevus Hereditary Hypophosphatemic Rickets Hypercalcemia, Infantile, 1 Hypercalciuria, Absorptive, 2 Hypercementosis Hyperparathyroidism Hyperphosphatemia Hypervitaminosis D Hypochondroplasia Hypophosphatasia Hypophosphatemia Hypophosphatemic Rickets and Hyperparathyroidism Hypophosphatemic Rickets, Autosomal Dominant Hypophosphatemic Rickets with Hypercalciuria, Hereditary Hypophosphatemic Rickets, X-Linked Dominant Idiopathic Hypercalciuria Idiopathic Infantile Hypercalcemia Insulin-Like Growth Factor I Kallmann Syndrome Mccune-Albright Syndrome Mineral Metabolism Disease Mitochondrial Complex I Deficiency Nephrocalcinosis Nephrolithiasis Nephrolithiasis, Calcium Oxalate Nephrolithiasis, X-Linked Recessive, with Renal Failure Nevus, Epidermal Occipital Horn Syndrome Oncogenic Osteomalacia Opsismodysplasia Osteomalacia Osteopetrosis Overhydrated Hereditary Stomatocytosis Papilledema Periodontitis Phacomatosis Pigmentokeratotica Phosphorus Metabolism Disease Precocious Puberty Pulmonary Alveolar Microlithiasis Raine Syndrome Ramer Ladda Syndrome Renal Osteodystrophy Rhabdomyosarcoma Rickets Schimmelpenning-Feuerstein-Mims Syndrome Secondary Hyperparathyroidism of Renal Origin Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Suppurative Periapical Periodontitis Synostosis Tetraamelia Syndrome, Autosomal Recessive Treacher Collins Syndrome 1 Turner Syndrome Vitamin D-Dependent Rickets, Type 2a