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autosomal recessive congenital ichthyosis 8 (DOID:0060717)
Alliance: disease page
Synonyms: ARCI8; lamellar ichthyosis 4; late-onset lamellar ichthyosis
Alt IDs: OMIM:613943, ICD10CM:Q80.2
Definition: An autosomal recessive congenital ichthyosis characterized by diffuse lamellar ichthyosis, slight facial erythema, hyperkeratosis, orthokeratosis, hypergranulosis, and acanthosis that has_material_basis_in homozygous mutation in the LIPN gene on chromosome 10q23.

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