| Human Disease |
Cutis Laxa, Neonatal, with Marfanoid Phenotype OMIM ID: 614100 |
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| Synonyms | Cutis Laxa-Marfanoid Syndrome | |||||||||||||||||||||
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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 06/12/2013 MGI 5.14 |
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