Hypodontia-dysplasia Of Nails Syndrome

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

Hypodontia-dysplasia Of Nails Syndrome Is also known as hypodontia-nail dysgenesis syndrome, tns, witkop syndrome, ectd3, ectodermal dysplasia 3, witkop type, nail dysplasia with hypodontia, tooth-and-nail syndrome, tooth and nail syndrome, ectodermal dysplasia 3, tooth/nail type.

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.

Hypodontia-dysplasia Of Nails Syndrome Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Orofacial cleft 5 (sequence analysis of MSX1 gene). By CGC Genetics (Portugal). MSX1 Specificity 100 % Genes 100 %
Ectodermal dysplasia (NGS panel for 8 genes). By CGC Genetics (Portugal). EDARADD, KRT74, EDAR, EDA, GJB6, HOXC13, KRT85, MSX1 Specificity 13 % Genes 100 %
Ectodermal dysplasia (NGS panel for 8 genes). By CGC Genetics (Portugal). EDARADD, KRT74, EDAR, EDA, GJB6, HOXC13, KRT85, MSX1 Specificity 13 % Genes 100 %
Ectodermal Dysplasia/Tooth Agenesis via MSX1 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). MSX1 Specificity 100 % Genes 100 %
Tooth Agenesis Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). WNT10A, EDARADD, EDAR, EDA, LTBP3, MSX1, PAX9, AXIN2 Specificity 13 % Genes 100 %
Cleft lip, cleft palate and related disorders NGS panel. By Connective Tissue Gene Tests (United States). BMP4, TBX22, SUMO1, TP63, TGDS, SATB2, COL11A1, COL11A2, COL9A1, COL9A2, COL9A3, GRHL3, FOXE1, IRF6, MSX1, NECTIN1 Specificity 7 % Genes 100 %
Cleft lip, cleft palate and related disorders Deletion / Duplication panel. By Connective Tissue Gene Tests (United States). BMP4, TBX22, SUMO1, TP63, TGDS, SATB2, COL11A1, COL11A2, COL9A1, COL9A2, COL9A3, GRHL3, FOXE1, IRF6, MSX1, NECTIN1 Specificity 7 % Genes 100 %
Cleft lip, cleft palate and related disorders Comprehensive panel. By Connective Tissue Gene Tests (United States). BMP4, TBX22, SUMO1, TP63, TGDS, SATB2, COL11A1, COL11A2, COL9A1, COL9A2, COL9A3, GRHL3, FOXE1, IRF6, MSX1, NECTIN1 Specificity 7 % Genes 100 %

Sources and references

You can check the following sources for additional information.

MESH OMIM ORPHANET Rare Disease Symptoms Checker

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