| Human Disease |
Ehlers-Danlos Syndrome, Type III OMIM ID: 130020 |
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| Synonyms | Benign Hypermobility Syndrome; Eds3; EDS III; Ehlers-Danlos Syndrome, Hypermobility Type | |||||||||||||||||||||||||
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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 05/08/2013 MGI 5.13 |
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