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Blepharocheilodontic syndrome 1

MONDO:0054740

Any blepharo-cheilo-odontic syndrome in which the cause of the disease is a mutation in the CDH1 gene.

Also known as: CDH1 blepharo-cheilo-odontic syndrome, blepharo-cheilo-odontic syndrome caused by mutation in CDH1, blepharocheilodontic syndrome 1, BCD syndrome, BCDS1, Lagophthalmia with bilateral cleft 51P and palate, blepharocheilodontic syndrome, clefting, ectropion, and conical teeth

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

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Disease (618) Hereditary disease (172) Skin disorder (123) Eye disorder (97) Syndromic disease (24) Human disease (14) Developmental defect during embryogenesis (7) Hereditary skin disorder (5) Disorder of orbital region (3) Ectodermal dysplasia syndrome (3)
Trials to join now! 13 Not yet recruiting 1 Not yet finished but already full! 2 Completed 3 Terminated 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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