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Autosomal recessive congenital ichthyosis 11

MONDO:0011218

Also known as: IFAH syndrome, IHS, autosomal recessive congenital ichthyosis 11, autosomal recessive congenital ichthyosis type 11, hypotrichosis-congenital ichthyosis syndrome, ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis, ichthyosis, congenital, autosomal recessive type 11, ichthyosis-follicular atrophoderma-hypotrichosis syndrome

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) Disease of genetic or genomic mechanism (2) Autosomal recessive congenital ichthyosis (1) Disease by body system or component (0)
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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