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Disease Ontology Browser
autosomal recessive congenital ichthyosis (DOID:0060655)
Alliance: disease page
Synonyms: ARCI; lamellar ichthyosis; non bullous congenital ichthyosiform erythroderma
Alt IDs: DOID:1696, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, DOID:1699, MESH:D016113, 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 (11)

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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last database update
02/18/2020
MGI 6.14
The Jackson Laboratory