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Article

Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes.

American journal of medical genetics. Part A - 1 Jul 2011

Bergendal Birgitta, Klar Joakim, Stecksén-Blicks Christina, Norderyd Johanna, Dahl Niklas

Abstract excerpt

Oligodontia is defined as the congenital lack of six or more permanent teeth, excluding third molars. Oligodontia as well as hypodontia (lack of one or more permanent teeth) are highly heritable conditions associated with mutations in the AXIN2, MSX1, PAX9, EDA, and EDAR genes. Here we define the prevalence of mutations in the AXIN2, MSX1, PAX9, EDA, and EDAR genes, and the novel candidate gene EDARADD in a...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21626677
DOI: 10.1002/ajmg.a.34045

Genes

EDARADD
AXIN2
MSX1
PAX9
EDA
EDAR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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