Autosomal recessive congenital ichthyosis 2
Autosomal recessive congenital ichthyosis 2
Definition
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 — per MONDO
Also identified as
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Integumental system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Skin of body | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |