| Human Disease |
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant OMIM ID: 130060 |
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| Synonyms | Arthrochalasis Multiplex Congenita; Eds Viia; EDS7A; Ehlers-Danlos Syndrome, Arthrochalasia 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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