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autosomal recessive congenital ichthyosis (DOID:0060655)
Alliance: disease page
Synonyms: ARCI; lamellar ichthyosis; non bullous congenital ichthyosiform erythroderma
Alt IDs: DOID:1696, ICD10CM:Q80.2, MESH:D017490, NCI:C84805, OMIM:PS242300, ORDO:281097, UMLS_CUI:C0079154
Definition: An ichthyosis that is characterized by autosomal recessive inheritance and abnormal skin scaling over the whole body due to a defect in keratinization.

Disease References using Mouse Models (12)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory