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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.
Term:hindlimb paralysis
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Accession:MP:0000755 term browser browse the term
Definition:severe or complete loss of power of voluntary movement in the muscles of the hindlimb through injury or disease of it or its nerve supply
Synonyms:exact_synonym: hind limb paralysis


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hindlimb paralysis term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atm ATM serine/threonine kinase IMP DNA:deletion:exon: RGD PMID:27895165 PMID:28007901 RGD:12879393, RGD:12879399 NCBI chr 8:53,828,741...53,932,773
Ensembl chr 8:53,831,093...53,932,437 		JBrowse link
G Atmem1Kyo ATM serine/threonine kinase; ZFN induced mutant 1, Kyo IMP RGD PMID:28007901 RGD:12879399
G Atmm1Kyo ATM serine/threonine kinase; ENU induced mutant 1, Kyo IMP RGD PMID:27895165 PMID:28007901 RGD:12879393, RGD:12879399
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  mammalian phenotype 5373
    behavior/neurological phenotype 582
      abnormal behavior 581
        abnormal motor capabilities/coordination/movement 224
          abnormal voluntary movement 151
            paralysis 12
              limb paralysis 8
                hindlimb paralysis 8
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