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dentin dysplasia type II
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
DSPP
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
regulation of odontoblast differentiation
odontoblast differentiation
dentinogenesis
hair follicle maturation
regulation of odontogenesis of dentin-containing tooth
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OMIM - Congenital disorder
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Literature
Most Relevant Literature
A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies.
A dentin sialophosphoprotein mutation that partially disrupts a splice acceptor site causes type II …
Identification of DSPP novel variants and phenotype analysis in dentinogenesis dysplasia Shields typ…
Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in COL1A2.
The Modified Shields Classification and 12 Families with Defined DSPP Mutations.
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Comparison of Autogenous Dentin Matrix Versus Bovine-Derived Xenograft for Socket Preservation
Effectiveness of Brush DJ App in Improving Oral Hygiene Compliance of Fixed Orthodontic Patients
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