| Human Disease |
Metaphyseal Chondrodysplasia, Schmid Type; MCDS OMIM ID: 156500 |
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| Synonyms | Spondylometaphyseal Dysplasia, Japanese Type | |||||||||||||||||||||
| 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 |
| Col10a1tm1.1Rpbh/Col10a1tm1.1Rpbh |
involves: 129/Sv * C57BL/6 | J:154052 | View |
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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