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Mammalian Phenotype Browser
Term Detail
MP term:abnormal synchondrosis
MP id: MP:0004053
Definition: anomalous or persistent cartilaginous fusion of two bones
Number of paths to term: 2

is-adenotes an 'is-a' relationship
part-ofdenotes a 'part-of' relationship


mammalian phenotype
        is-askeleton phenotype
                is-aabnormal skeleton morphology
                        is-aabnormal cartilage morphology
                                is-aabnormal cartilage development
                                        is-aabnormal intervertebral disk development
                                        is-aabnormal long bone epiphyseal plate proliferative zone
                                        is-aabnormal long bone hypertrophic chondrocyte zone +
                                        is-aabnormal synchondrosis [MP:0004053] (9 genotypes, 9 annotations)


mammalian phenotype
        is-askeleton phenotype
                is-aabnormal skeleton morphology
                        is-aabnormal skeleton development
                                is-aabnormal cartilage development
                                        is-aabnormal intervertebral disk development
                                        is-aabnormal long bone epiphyseal plate proliferative zone
                                        is-aabnormal long bone hypertrophic chondrocyte zone +
                                        is-aabnormal synchondrosis [MP:0004053] (9 genotypes, 9 annotations)

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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
09/09/2014
MGI 5.19
The Jackson Laboratory