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Up to: Autosomal recessive congenital ichthyosis · Lamellar ichthyosis
Autosomal recessive congenital ichthyosis 5
An autosomal recessive congenital ichthyosis characterized by fine white or greyish-white scales, hyperkeratosis, moderate acanthosis, and moderate parakeratosis that has material basis in homozygous mutation in the CYP4F22 gene on chromosome 19p13.
This condition has no sub-types.