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Human Disease and Mouse Model Detail
Human Disease Chondrodysplasia Punctata 2, X-Linked Dominant; CDPX2
OMIM ID: 302960
Synonyms CDPXD; CPXD; Chondrodysplasia Punctata; Conradi-Hunermann Syndrome; Conradi-Hunermann-Happle Syndrome; Happle Syndrome
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Ebp* EBP* View 1 model 1:1 Homology
     Nsdhl* NSDHL View 1 model 1:1 Homology
References Disease References using Mouse Models (2)

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
11/18/2014
MGI 5.20
The Jackson Laboratory