| Human Disease |
Cutis Laxa, Autosomal Recessive, Type Ic; ARCL1C OMIM ID: 613177 |
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| Synonyms | Cutis Laxa with Severe Pulmonary, Gastrointestinal, and Urinary Abnormalities; Urban-Rifkin-Davis Syndrome; URDS | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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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 06/05/2013 MGI 5.13 |
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