Mutations in these genes lead to human genetic skin diseases such as epidermolytic hyperkeratosis (KRT1), ichthyosis vulgaris (FLG), seborrheic dermatitis (ZNF750), psoriasis (LCE3D), and harlequin ichthyosis (ABCA12) [20–24]. The gene discussed is ABCA12; the disease is epidermolytic ichthyosis.