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Autosomal recessive congenital ichthyosis 4A

MONDO:0011026

Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the ABCA12 gene.

Also known as: ARCI4A, ICR2B, autosomal recessive congenital ichthyosis type 4A, ichthyosis, congenital, autosomal recessive type 4A, LI2, ichthyosis congenita 2B, ichthyosis lamellar 2, ichthyosis, congenital, autosomal recessive 4A

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

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Sub-types

Autosomal recessive congenital ichthyosis 4B (0)

Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Eye disorder (97) Human disease (14) Ichthyosis (11) Hereditary skin disorder (5) Inherited ichthyosis (5) Lamellar ichthyosis (4) Disorder of orbital region (3)
Trials to join now! 11 Not yet recruiting 1 Not yet finished but already full! 3 Completed 2 Terminated 2
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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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