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Mammalian Phenotype Browser
Term Detail
MP term:paralysis
MP id: MP:0000753
Definition: loss of power of voluntary movement in a muscle through injury or disease of its nerve supply
Number of paths to term: 1

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


mammalian phenotype
        is-abehavior/neurological phenotype
                is-aabnormal behavior
                        is-aabnormal motor capabilities/coordination/movement
                                is-aabnormal voluntary movement
                                        is-aabnormal locomotor behavior +
                                        is-aabnormal stationary movement +
                                        is-adecreased gnawing activity
                                        is-aincreased gnawing activity
                                        is-aparalysis [MP:0000753] (254 genotypes, 272 annotations)
                                                is-acarpoptosis
                                                is-aforelimb paralysis
                                                is-ahindlimb paralysis
                                                is-alimb paralysis
                                        is-aparesis
                                        is-aslow movement
                                        is-aspasticity +

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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
07/15/2014
MGI 5.18
The Jackson Laboratory