Autosomal recessive congenital ichthyosis 2

MONDO:0009439

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.

Also known as: ARCI2, autosomal recessive congenital ichthyosis type 2, ichthyosis, congenital, autosomal recessive type 2, NBCIE, NCIE, collodion baby, self-healing, ichthyosiform erythroderma, Brocq congenital, nonbullous form, ichthyosiform erythroderma, Brocq congenital, nonbullous form, formerly

3 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive congenital ichthyosis 2 itself.

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↑ Congenital non-bullous ichthyosiform erythroderma (1) ↑ Self-healing collodion baby (0)

Including sub-types (3) Tagged with Autosomal recessive congenital ichthyosis 2 (0)

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