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Disease Ontology Browser
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.


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
07/02/2024
MGI 6.13
The Jackson Laboratory