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Autosomal recessive congenital ichthyosis 7

MONDO:0014009

An autosomal recessive congenital ichthyosis characterized by fine whitish scales, moderate to severe erythroderma, compact hyperkeratosis, hypergranulosis, acanthosis, and papillomatosis that has material basis in variation in the chromosome region 12p11.2-q13.1.

Also known as: ARCI7, autosomal recessive congenital ichthyosis type 7, ichthyosis, congenital, autosomal recessive 7

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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