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Autosomal recessive congenital ichthyosis 8

MONDO:0013495

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

Also known as: ARCI8, autosomal recessive congenital ichthyosis type 8, ichthyosis, congenital, autosomal recessive type 8, ichthyosis, congenital, autosomal recessive 8, ichthyosis, lamellar, 4, ichthyosis, lamellar, 4, formerly, lamellar ichthyosis, late-onset

3 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive congenital ichthyosis 8 itself.

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