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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
Mouse Phenotypes - Amelogenesis imperfecta
OMIM - Skeletal and Integument Related Disorders
OMIM - Trichodontoosseous syndrome
OMIM - Kohlschutter-Tonz syndrome
OMIM - Congenital disorder
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Literature
Most Relevant Literature
Molecular-based phenotype variations in amelogenesis imperfecta.
A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance.
Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta.
The implication of holocytochrome c synthase mutation in Korean familial hypoplastic amelogenesis im…
Age-related dental phenotypes and tooth characteristics of FAM83H-associated hypocalcified amelogene…
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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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