Autosomal recessive congenital ichthyosis 8
MONDO:0013495Any 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
19 clinical trials for this condition and its sub-types.
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