Hypohidrotic Ectodermal Dysplasia

About the Disease
Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive, also known as hypohidrotic ectodermal dysplasia, is related to immunodeficiency 33 and ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant, and has symptoms including dyspnea, dry skin and koilonychia. An important gene associated with Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive is EDAR (Ectodysplasin A Receptor), and among its related pathways/superpathways are Innate Immune System and Signal Transduction. The drugs Antibodies and Immunoglobulins, Intravenous have been mentioned in the context of this disorder. Affiliated tissues include skin, eye and breast, and related phenotypes are abnormal facial shape and thick vermilion border

Common Targets
EDARADD | EDA | IKBKG | NFKBIA | DSP | EDAR | GJB6 | WDR35 | WNT10A | SMARCAD1 | TSPEAR

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