has material basis in germline mutation in CYP4F22 autosomal recessive congenital ichthyosis 5 https://github.com/monarch-initiative/mondo/issues/4069 https://rarediseases.info.nih.gov/diseases/9734/ichthyosis-lamellar-3 https://www.malacards.org/card/ichthyosis_congenital_autosomal_recessive_5 GARD:0009734 ARCI5 MESH:C537265 UMLS:C1858133 NNCI autosomal recessive congenital ichthyosis type 5 type 3 lamellar ichthyosis ichthyosis, congenital, autosomal recessive type 5 ichthyosis lamellar 3 lamellar ichthyosis, type 3 MEDGEN:347628 ichthyosis, lamellar, 3, formerly ichthyosis congenita 3 MONDO:0011485 autosomal recessive congenital ichthyosis 5 ichthyosis, lamellar, 3 ichthyosis, NONLAMELLAR and NONERYTHRODERMIC, congenital, autosomal recessive OMIM:604777 ichthyosis congenita III LI3, formerly DOID:0060714 An autosomal recessive congenital ichthyosis characterized by fine white or greyish-white scales, hyperkeratosis, moderate acanthosis, and moderate parakeratosis that has material basis in homozygous mutation in the CYP4F22 gene on chromosome 19p13. ichthyosis, congenital, autosomal recessive 5 autosomal recessive congenital ichthyosis lamellar ichthyosis