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Human Disease and Mouse Model Detail
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| Human Disease | Term: Ichthyosis, Congenital, Autosomal Recessive 1; ARCI1 |
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| Synonyms | Collodion Baby, Self-Healing; SHCB; Collodion Fetus; Desquamation of Newborn; Ichthyosis Congenita; Ichthyosis Congenita II; ICR2; Ichthyosis, Congenital, Autosomal Recessive 1, with Bathing Suit Distribution; Ichthyosis, Lamellar, 1, Formerly; LI1, FORMERLY; Lamellar Exfoliation of Newborn | |||||||||||||||||||
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
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Mouse Models |
1Human genes are associated with this disease. Mouse model genotypes include mutations in the orthologs of these human genes. |
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 04/03/2013 MGI 5.12 |
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