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Disease Ontology Browser
autosomal recessive congenital ichthyosis 3 (DOID:0060711)
Synonyms: ARCI3; lamellar ichthyosis 5
Alt IDs: OMIM:606545, ICD10CM:Q80.2
Definition: An autosomal recessive congenital ichthyosis characterized by mild ichthyosis, fine scales on the scalp, face, trunk and limbs, dark brown adherent scales on the neck, elbow and knees, and hypohydrosis that has_material_basis_in homozygous or compound heterozygous mutation in the ALOXE3 gene on chromosome 17p13.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory