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amelogenesis imperfecta
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
AIH3
ENAM
SP6
AMTN
RELT
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
OMIM - Kohlschutter-Tonz syndrome
OMIM - Trichodontoosseous syndrome
OMIM - Skeletal and Integument Related Disorders
OMIM - Kidney disease
Mouse Phenotypes - Amelogenesis imperfecta
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Literature
Most Relevant Literature
Digenic inheritance accounts for phenotypic variability in amelogenesis imperfecta.
Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta.
Molecular-based phenotype variations in amelogenesis imperfecta.
Association between malocclusions and amelogenesis imperfecta genotype and phenotype: A systematic r…
Oro-dental phenotyping and report of three families with RELT-associated amelogenesis imperfecta.
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Clinical Trials
Most Relevant Clinical Trials
Psycho-social Impact of Amelogenesis and Dentinogenesis Imperfecta
Amelogenesis Imperfecta
Dental Age Estimation by Different Methods in Patients With Amelogenesis Imperfecta
Clinical Performance of Composites in Patients With Amelogenesis Imperfecta
E. Max Laminate Veneers With and Without Using Galla Chinnesis as Natural Cross Linking and Reminera…
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