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Human Disease and Mouse Model Detail
Human Disease Paget Disease, Juvenile
OMIM ID: 239000
Synonyms Hyperostosis Corticalis Deformans Juvenilis; Hyperphosphatasemia, Chronic Congenital Idiopathic; Hyperphosphatasia, Familial Idiopathic; Juvenile Paget Disease; JPD; Osteoectasia, Familial
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     TNFRSF11B* Tnfrsf11b   HomoloGene

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/20/2015
MGI 5.22
The Jackson Laboratory