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Disease Ontology Browser
autosomal recessive congenital ichthyosis 5 (DOID:0060714)
Synonyms: ARCI5; autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis
Alt IDs: OMIM:604777, ICD10CM:Q80.2, ORDO:313
Definition: An autosomal recessive congenital ichthyosis characterized by fine white or greyish-white scales, hyperkeratosis, moderate acanthosis, and moderate parakeratosis that has_material_basis_in homozygous mutation in the CYP4F22 gene on chromosome 19p13.

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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 6.08
The Jackson Laboratory