Oligodontia

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Description

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

Genes related to Oligodontia

EDARADD
IRF6
WNT10A
AXIN2
MSX1
FGFR1
WNT10B
SUMO1
TGFA
LRP6
EDA
PAX9

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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.

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.

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