Hair Morphology 1; Hrm1

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 Hair Morphology 1; Hrm1

EDAR

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

Hair Morphology 1; Hrm1 Is also known as hair thickness, variation in.

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.

Hair Morphology 1; Hrm1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
EDAR. By Institute for Human Genetics University Clinic Freiburg (Germany). EDAR Specificity 100 % Genes 100 %
EDAR Gene Sequencing. By GeneDx (United States). EDAR 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 %
EDAR. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). EDAR 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 %
Anhidrotic ectodermal dysplasia (sequence analysis of EDAR gene). By CGC Genetics (Portugal). EDAR 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 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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