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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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.12
The Jackson Laboratory