autosomal recessive congenital ichthyosis 7 Disease Ontology Browser

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Disease Ontology Browser

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.

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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