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enamel hypoplasia
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
AIH3
ENAM
SP6
AMTN
SLC10A7
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
odontogenesis
biomineral tissue development
regulation of animal organ morphogenesis
amelogenesis
regulation of odontogenesis of dentin-containing tooth
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Amelogenesis imperfecta
OMIM - Congenital disorder
OMIM - Skeletal and Integument Related Disorders
OMIM - Kohlschutter-Tonz syndrome
OMIM - Heimler syndrome
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Literature
Most Relevant Literature
The role of FGF9-mediated TGF-β1/Smad signaling in enamel hypoplasia induced by exposure to fluoride…
Toward Preventing Enamel Hypoplasia: Modeling Maternal and Neonatal Biomarkers of Human Calcium Home…
Tmem2 Deficiency Leads to Enamel Hypoplasia and Soft Enamel in Mouse.
Gestational Serum Retinol Deficiency Is Associated with Enamel Hypoplasia.
Association Between Molar-Incisor Hypomineralization and Enamel Hypoplasia.
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Clinical Trials
Most Relevant Clinical Trials
Colorimetric, Ultra-structural and Elemental Comparison of Dental Enamel Defects
Caries Prevention Potential of Pearl Powder Versus CPP-ACP on Enamel White Spot Lesions
Evaluation of Enamel Demineralization During Clear Aligner Orthodontic Treatment
Laser Used in the Treatment of Hypomineralized Occlusal Lesions in Teeth Enamel Affected by MIH
Evaluation of CPP-ACP Prophylactic Effect on Enamel Surface During Orthodontic Treatment
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