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Human Disease and Mouse Model Detail
Human Disease Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome; CACP
OMIM ID: 208250
Synonyms Arthropathy-Camptodactyly Syndrome; Camptodactyly-Arthropathy-Pericarditis Syndrome; CAP Syndrome; Fibrosing Serositis, Familial; Hypertrophic Synovitis, Congenital Familial; Jacobs Syndrome; PAC Syndrome; Pericarditis-Arthropathy-Camptodactyly Syndrome
View all models View ALL (1) 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
     Prg4* View 1 model 1:0 Homology
     PRG4*   0:1 Homology
References Disease References using Mouse Models (1)

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
09/09/2014
MGI 5.19
The Jackson Laboratory