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241500	-	HYPOPHOSPHATASIA, INFANTILE

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Musculoskeletal Diseases

Bone Diseases, Developmental

Osteochondrodysplasias

Cleidocranial Dysplasia

Bone Diseases, Metabolic

Osteitis Deformans

Spinal Diseases

Spinal Curvatures

Musculoskeletal Abnormalities

Craniofacial Abnormalities

Cleidocranial Dysplasia

Rheumatic Diseases

Stomatognathic Diseases

Tooth Resorption

Nervous System Diseases

Central Nervous System Diseases

Neurologic Manifestations

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

Pregnancy Complications

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Congenital Abnormalities

Musculoskeletal Abnormalities

Craniofacial Abnormalities

Cleidocranial Dysplasia

Genetic Diseases, Inborn

Metabolism, Inborn Errors

Metal Metabolism, Inborn Errors

Hypophosphatasia

Hypophosphatemia, Familial

Purine-Pyrimidine Metabolism, Inborn Errors

Renal Tubular Transport, Inborn Errors

Hypophosphatemia, Familial

Nutritional and Metabolic Diseases

Metabolic Diseases

Calcium Metabolism Disorders

Metabolism, Inborn Errors

Metal Metabolism, Inborn Errors

Hypophosphatasia

Hypophosphatemia, Familial

Purine-Pyrimidine Metabolism, Inborn Errors

Renal Tubular Transport, Inborn Errors

Hypophosphatemia, Familial

Phosphorus Metabolism Disorders

Hypophosphatemia

Hypophosphatemia, Familial

Water-Electrolyte Imbalance

Pathological Conditions, Signs and Symptoms

Pathologic Processes

Chromosome Aberrations

Chromosome Deletion

Disease Attributes

Diseases in Twins

Signs and Symptoms

Neurologic Manifestations

Wounds and Injuries

Fractures, Bone

Fractures, Spontaneous

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