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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

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

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Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Human disease (14) Ichthyosis (12) Hereditary skin disorder (6) Inherited ichthyosis (6) Autosomal recessive congenital ichthyosis (2) Disease of genetic or genomic mechanism (2) Disease by body system or component (0)
Not yet finished but already full! 1 Completed 1 Terminated 1
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  • Scientists hunt for clues to ichthyosis in skin and blood

    Knowledge-focused ENROLLING_BY_INVITATION

    This study looks at skin and blood samples from 200 people with ichthyosis (a genetic condition causing dry, scaly skin) and healthy volunteers. Researchers want to find specific markers that could help them understand the disease better and develop new treatments. No treatment i…

    Sponsor: Northwestern University • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:25 UTC

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