has material basis in germline mutation in ALOX12B autosomal recessive congenital ichthyosis 2 https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/ichthyosis_congenital_autosomal_recessive_2 ichthyosis, congenital, autosomal recessive type 2 NBCIE autosomal recessive congenital ichthyosis type 2 MEDGEN:854762 ichthyosiform erythroderma, Brocq congenital, nonbullous form MONDO:0009439 DOID:0060710 OMIM:242100 ichthyosis, congenital, autosomal recessive 2 NCIE NCIT:C132827 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. ichthyosiform erythroderma, congenital, nonbullous, 1 ARCI2 GARD:0015187 ichthyosiform erythroderma, nonbullous congenital, 1 UMLS:C3888093 self-healing collodion baby congenital non-bullous ichthyosiform erythroderma