Oligodontia

Description

Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth.

Clinical Features

Phenotypes and symptoms related to Oligodontia

  • Micrognathia
  • Hypoplasia of the maxilla
  • Microdontia
  • Abnormality of the face
  • Oligodontia
  • Abnormality of dental morphology

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Oligodontia Is also known as selective tooth agenesis.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.


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Oligodontia Recommended genes panels

Panel Name, Specifity and genes Tested/covered
EDARADD Gene Sequencing.

By GeneDx (United States).

EDARADD
Specificity
100 %
Genes
9 %
TP63,EDA,EDAR,EDARADD,WNT10A, NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

WNT10A, EDARADD, TP63, EDAR, EDA
Specificity
60 %
Genes
25 %
EDARADD. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

EDARADD
Specificity
100 %
Genes
9 %
Ectodermal dysplasia 1, hypohidrotic, X-linked (deletion/duplication analysis of genes EDA, EDAR, EDARADD and WNT10A).

By CGC Genetics (Portugal).

WNT10A, EDARADD, EDAR, EDA
Specificity
75 %
Genes
25 %
Anhidrotic ectodermal dysplasia (sequence analysis of EDARADD gene).

By CGC Genetics (Portugal).

EDARADD
Specificity
100 %
Genes
9 %
Ectodermal dysplasia (NGS panel for 8 genes).

By CGC Genetics (Portugal).

EDARADD, KRT74, EDAR, EDA, GJB6, HOXC13, KRT85, MSX1
Specificity
38 %
Genes
25 %
Ectodermal dysplasia (NGS panel for 8 genes).

By CGC Genetics (Portugal).

EDARADD, KRT74, EDAR, EDA, GJB6, HOXC13, KRT85, MSX1
Specificity
38 %
Genes
25 %
Ectodermal Dysplasia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

WNT10A, EDARADD, EDAR, EDA, KRT85, NECTIN1
Specificity
50 %
Genes
25 %

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Sources and references

You can check the following sources for additional information.

ORPHANET Rare Disease Symptoms Checker

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