Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Autosomal recessive congenital ichthyosis 3

MONDO:0011680

Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the ALOXE3 gene.

Also known as: ARCI3, autosomal recessive congenital ichthyosis type 3, ichthyosis, congenital, autosomal recessive type 3, collodion baby, self-healing, ichthyosis, congenital, autosomal recessive 3, ichthyosis, lamellar, 5, ichthyosis, lamellar, 5, formerly

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

Follow this condition — get notified about new trials

Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Eye disorder (102) Human disease (14) Ichthyosis (12) Hereditary skin disorder (6) Inherited ichthyosis (6) Autosomal recessive disease (4) Lamellar ichthyosis (4)
Not yet finished but already full! 1 Completed 1 Terminated 1
Sort by
  • 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

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space