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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 - Skeletal and Integument Related Disorders
OMIM - Kohlschutter-Tonz syndrome
OMIM - Heimler syndrome
OMIM - Congenital disorder
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Literature
Most Relevant Literature
An intronic variant in LAMB3 contributes to junctional epidermolysis bullosa and enamel hypoplasia v…
The role of FGF9-mediated TGF-β1/Smad signaling in enamel hypoplasia induced by exposure to fluoride…
Enamel hypoplasia: a potential diagnostic aid in DiGeorge syndrome.
Toward Preventing Enamel Hypoplasia: Modeling Maternal and Neonatal Biomarkers of Human Calcium Home…
Tmem2 Deficiency Leads to Enamel Hypoplasia and Soft Enamel in Mouse.
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Clinical Trials
Most Relevant Clinical Trials
Injection Molding Technique: a Minimally Invasive Management for Enamel Hypoplasia Affecting Permane…
Colorimetric, Ultra-structural and Elemental Comparison of Dental Enamel Defects
Preventive Effects of Silver Diamine Fluoride on Early Enamel Caries
Caries Prevention Potential of Pearl Powder Versus CPP-ACP on Enamel White Spot Lesions
The Remineralization of Early Enamel Caries in Permanent Teeth
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