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X-linked hypohidrotic ectodermal dysplasia

MONDO:0010585

An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ectodysplasin.

Also known as: Christ-Siemens-Touraine syndrome, X-linked hypohidrotic ectodermal dysplasia, XHED, ectodermal dysplasia 1, hypohidrotic, X-linked, X-linked recessive, hypohidrotic ectodermal dysplasia, X-linked, CST syndrome, Eda1, Xlhed

7 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Syndromic disease (24) X-linked disease (16) Human disease (14) Hereditary skin disorder (5) Ectodermal dysplasia syndrome (3) Disease of genetic or genomic mechanism (2) Hypohidrotic ectodermal dysplasia (1)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
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  • Skin deep: european study probes the hidden emotional toll of skin diseases

    Knowledge-focused Not yet recruiting

    This study looks at how people with skin conditions (like eczema, psoriasis, or skin cancer) manage stress, feel lonely, and bounce back from challenges. Researchers will compare 375 adults with and without skin disease across 15 European countries using questionnaires. The goal …

    Phase: NA • Sponsor: University Hospital, Brest • Aim: Knowledge-focused

    Last updated Jun 27, 2026 13:06 UTC

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