| Human Disease |
Epiphyseal Dysplasia, Multiple, 5; EDM5 OMIM ID: 607078 |
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| Synonyms | Microepiphyseal Dysplasia, Bilateral Hereditary; BHMED; Multiple Epiphyseal Dysplasia, MATN3-Related | |||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Matn3tm1Mbri/Matn3tm1Mbri |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:125104 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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