About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Ichthyosis, Congenital, Autosomal Recessive 5; ARCI5
OMIM ID: 604777
Human Phenotype Ontology associations
Synonyms Ichthyosis Congenita III; Ichthyosis, Congenital, Autosomal Recessive; Ichthyosis, Lamellar, 3, Formerly; LI3, FORMERLY; Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive; NNCI
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

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
MGI 6.07
The Jackson Laboratory