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239000	-	PAGET DISEASE, JUVENILE

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Musculoskeletal Diseases

Bone Diseases, Developmental

Osteochondrodysplasias

Fibrous Dysplasia of Bone

Hyperostosis, Cortical, Congenital

Bone Diseases, Endocrine

Osteitis Fibrosa Cystica

Bone Diseases, Metabolic

Bone Resorption

Hyperostosis, Cortical, Congenital

Osteitis Deformans

Nervous System Diseases

Neurologic Manifestations

Neurobehavioral Manifestations

Intellectual Disability

Psychomotor Disorders

Male Urogenital Diseases

Urologic Diseases

Kidney Diseases

Renal Tubular Transport, Inborn Errors

Hypophosphatemia, Familial

Female Urogenital Diseases and Pregnancy Complications

Female Urogenital Diseases

Urologic Diseases

Kidney Diseases

Renal Tubular Transport, Inborn Errors

Hypophosphatemia, Familial

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Genetic Diseases, Inborn

Metabolism, Inborn Errors

Metal Metabolism, Inborn Errors

Hypophosphatemia, Familial

Renal Tubular Transport, Inborn Errors

Hypophosphatemia, Familial

Infant, Newborn, Diseases

Hyperostosis, Cortical, Congenital

Nutritional and Metabolic Diseases

Metabolic Diseases

Metabolism, Inborn Errors

Metal Metabolism, Inborn Errors

Hypophosphatemia, Familial

Renal Tubular Transport, Inborn Errors

Hypophosphatemia, Familial

Phosphorus Metabolism Disorders

Hypophosphatemia

Hypophosphatemia, Familial

Pathological Conditions, Signs and Symptoms

Pathologic Processes

Disease Attributes

Chronic Disease

Signs and Symptoms

Neurologic Manifestations

Neurobehavioral Manifestations

Intellectual Disability

Psychomotor Disorders

Wounds and Injuries

Fractures, Bone

Fractures, Spontaneous

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