Tooth Agenesis, Selective, X-linked, 1; Sthagx1

Table of contents:

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

Genes related to Tooth Agenesis, Selective, X-linked, 1; Sthagx1

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Clinical Features

Top most frequent phenotypes and symptoms related to Tooth Agenesis, Selective, X-linked, 1; Sthagx1

Hyperhidrosis
Hypodontia
Ectodermal dysplasia
Oligodontia
Anodontia
Heat intolerance
Hypohidrotic ectodermal dysplasia
Agenesis of premolar
Agenesis of molar
Agenesis of lateral incisor

And another 1 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— The onset for some of the known clinical features related to this disease may vary, including juvenile onset .

Alternative names

Tooth Agenesis, Selective, X-linked, 1; Sthagx1 Is also known as hypodontia/oligodontia, x-linked, 1.

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.

Tooth Agenesis, Selective, X-linked, 1; Sthagx1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
EDA Sequencing. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). EDA Specificity 100 % Genes 100 %
EDA. By Institute for Human Genetics University Clinic Freiburg (Germany). EDA Specificity 100 % Genes 100 %
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 20 % Genes 100 %
EDA. MLPA testing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). EDA Specificity 100 % Genes 100 %
EDA. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). EDA Specificity 100 % Genes 100 %
Hypohidrotic ectodermal dysplasia 1, X-linked (sequence analysis of EDA gene). By CGC Genetics (Portugal). EDA Specificity 100 % Genes 100 %
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 25 % Genes 100 %
Hypohidrotic ectodermal dysplasia 1, X-linked (sequence analysis of EDA gene). By CGC Genetics (Portugal). EDA Specificity 100 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Symptoms Checker

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