Condition: Hypodontia


rs2034604 in ARHGAP15 gene and Hypodontia PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs4498834 in CACNA1S gene and Hypodontia PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs397516654 in EDA gene and Hypodontia PMID 19623212 2010 Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis.

PMID 24487376 2014 Oligodontia and curly hair occur with ectodysplasin-a mutations.

PMID 19278982 2009 EDA gene mutations underlie non-syndromic oligodontia.

rs35956082 in FOXP1 gene and Hypodontia PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs515726227 in MSX1 gene and Hypodontia PMID 24914010 2014 In this study, we identified a novel heterozygous non-stop mutation (c.910_911dupTA, p.*304Tyrext*48) in MSX1 in a Chinese family with autosomal dominant non-syndromic oligodontia.

PMID 8696335 1996 A human MSX1 homeodomain missense mutation causes selective tooth agenesis.

rs758468472 in NOL11;LOC101928045 gene and Hypodontia PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs1555316704 in PAX9;LOC105370455 gene and Hypodontia PMID 22581971 2012 Mutations in WNT10A are present in more than half of isolated hypodontia cases.

rs797044484 in TP63 gene and Hypodontia PMID 19903181 2010 Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlation.

rs121908120 in WNT10A gene and Hypodontia PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.