Tooth Agenesis, Selective, 4; Sthag4

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, 4; Sthag4

WNT10A

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Tooth Agenesis, Selective, 4; Sthag4

Sparse hair
Dry skin
Hypodontia
Reduced number of teeth
Sparse eyebrow
Agenesis of permanent teeth
Anodontia
Conical incisor
Short eyelashes
Peg-shaped maxillary lateral incisors

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

Tooth Agenesis, Selective, 4; Sthag4 Is also known as tooth agenesis, selective, 4, with or without ectodermal dysplasia, lateral incisors, absence of, succedaneous teeth, agenesis of, lateral incisors, pegged or missing.

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, 4; Sthag4 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
WNT10A. By Institute for Human Genetics University Clinic Freiburg (Germany). WNT10A Specificity 100 % Genes 100 %
WNT10A Gene Sequencing. By GeneDx (United States). WNT10A 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 %
WNT10A. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). WNT10A Specificity 100 % Genes 100 %
Odontoonychodermal dysplasia (sequence analysis of WNT10A gene). By CGC Genetics (Portugal). WNT10A 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 %
Ectodermal Dysplasia Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). WNT10A, EDARADD, EDAR, EDA, KRT85, NECTIN1 Specificity 17 % Genes 100 %
Ectodermal Dysplasia via WNT10A Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). WNT10A Specificity 100 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

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