Autosomal recessive congenital ichthyosis 6

MONDO:0012847

Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the NIPAL4 gene.

Also known as: ARCI6, autosomal recessive congenital ichthyosis type 6, ichthyosis, congenital, autosomal recessive type 6, ichthyosis, congenital, autosomal recessive 6, ichthyosis, congenital, autosomal recessive, Nipal4-related

4 clinical trials for this condition and its sub-types, 1 tagged with Autosomal recessive congenital ichthyosis 6 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Lamellar ichthyosis (4) ↑ Congenital non-bullous ichthyosiform erythroderma (1)

Including sub-types (4) Tagged with Autosomal recessive congenital ichthyosis 6 (1)

Not yet recruiting 1

Rare skin disease patients develop even rarer lymphoma – scientists investigate why

Knowledge-focused Not yet recruiting

This study looks at the blood immune cells of 10 adults with a rare inherited skin condition called NIPAL4 ichthyosis. Researchers want to understand why three patients with this skin disease also developed a very rare lymphoma (Sezary syndrome). By describing the normal immune c…

Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused

Last updated Jun 27, 2026 11:02 UTC

Autosomal recessive congenital ichthyosis 6

Where it sits in the disease tree

Rare skin disease patients develop even rarer lymphoma – scientists investigate why