autosomal recessive congenital ichthyosis 7 (DOID:0060716)
Alliance: disease page
Synonyms: ARCI7
Alt IDs: OMIM:615022, ICD10CM:Q80.2
Definition: An autosomal recessive congenital ichthyosis characterized by fine whitish scales, moderate to severe erythroderma, compact hyperkeratosis, hypergranulosis, acanthosis, and papillomatosis that has_material_basis_in variation in the chromosome region 12p11.2-q13.1.