About   Help   FAQ
Mammalian Phenotype Browser
Term Detail
MP term:spina bifida
Synonym: spinal dysraphism
MP id: MP:0003054
Alternate id: Fyler:4157
Definition: common congenital midline defect of fusion of the vertebral arch
Number of paths to term: 2

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


mammalian phenotype
        is-aembryo phenotype
                is-aabnormal embryo morphology
                        is-aabnormal embryonic tissue morphology
                                is-aabnormal neural tube morphology
                                        is-aabnormal neural tube closure
                                                is-aopen neural tube
                                                        is-aspina bifida [MP:0003054] (172 genotypes, 182 annotations)
                                                                is-aspina bifida cystica +
                                                                is-aspina bifida occulta +


mammalian phenotype
        is-anervous system phenotype
                is-aabnormal nervous system morphology
                        is-aabnormal nervous system development
                                is-aabnormal neural tube morphology
                                        is-aabnormal neural tube closure
                                                is-aopen neural tube
                                                        is-aspina bifida [MP:0003054] (172 genotypes, 182 annotations)
                                                                is-aspina bifida cystica +
                                                                is-aspina bifida occulta +

Back to entry page

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
06/22/2016
MGI 6.04
The Jackson Laboratory