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Autosomal recessive congenital ichthyosis 9

MONDO:0014010

Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the CERS3 gene.

Also known as: ARCI9, autosomal recessive congenital ichthyosis 9, autosomal recessive congenital ichthyosis type 9, ichthyosis, congenital, autosomal recessive type 9, ichthyosis, congenital, autosomal recessive 9

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

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Human disease (14) Ichthyosis (11) Hereditary skin disorder (5) Inherited ichthyosis (5) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal recessive congenital ichthyosis (1)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 2 Completed 2 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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