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Autosomal recessive congenital ichthyosis 2
rareAn 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.
- Identifiers
- MONDO:0009439 OMIM:242100
- Causal genes
- ALOX12B
- Also known as
- ARCI2 · autosomal recessive congenital ichthyosis type 2 · ichthyosiform erythroderma, Brocq congenital, nonbullous form · ichthyosiform erythroderma, congenital, nonbullous, 1 · ichthyosiform erythroderma, nonbullous congenital, 1
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