MeSH Treeview
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104500
AIH2
AMELOGENESIS IMPERFECTA 2, HYPOPLASTIC LOCAL, AUTOSOMAL DOMINANT
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Metabolic
Pseudohypoparathyroidism
Stomatognathic Diseases
Stomatognathic System Abnormalities
Tooth Abnormalities
Dental Enamel Hypoplasia
Amelogenesis Imperfecta
Odontodysplasia
Tooth Diseases
Malocclusion
Tooth Abnormalities
Dental Enamel Hypoplasia
Amelogenesis Imperfecta
Odontodysplasia
Tooth Discoloration
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Skin Abnormalities
Epidermolysis Bullosa
Stomatognathic System Abnormalities
Tooth Abnormalities
Dental Enamel Hypoplasia
Amelogenesis Imperfecta
Odontodysplasia
Genetic Diseases, Inborn
Chromosome Disorders
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Pseudohypoparathyroidism
Skin Diseases, Genetic
Epidermolysis Bullosa
Skin and Connective Tissue Diseases
Skin Diseases
Skin Abnormalities
Epidermolysis Bullosa
Skin Diseases, Genetic
Epidermolysis Bullosa
Skin Diseases, Vesiculobullous
Epidermolysis Bullosa
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Pseudohypoparathyroidism
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Pseudohypoparathyroidism
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Growth Disorders
Hyperplasia
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