DO_rare_slim disease has basis in autosomal recessive congenital ichthyosis autosomal recessive congenital ichthyosis 3 ICD10CM:Q80.2 MIM:606545 disease_ontology DOID:0060711 ARCI3 An autosomal recessive congenital ichthyosis characterized by mild ichthyosis, fine scales on the scalp, face, trunk and limbs, dark brown adherent scales on the neck, elbow and knees, and hypohydrosis that has_material_basis_in homozygous or compound heterozygous mutation in the ALOXE3 gene on chromosome 17p13. lamellar ichthyosis 5 Abnormality of prenatal development or birth