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Up to: Congenital non-bullous ichthyosiform erythroderma · Self-healing collodion baby
Autosomal recessive congenital ichthyosis 2
An autosomal recessive condition caused by mutation(s) in the ALOX12B gene, encoding arachidonate 12-lipoxygenase, 12R-type. It is characterized by dry, thickened, scaly skin.
This condition has no sub-types.