About   Help   FAQ
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
11/07/2017
MGI 6.11
The Jackson Laboratory