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Human Disease and Mouse Model Detail
Human Disease Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome; CACP
OMIM ID: 208250
Human Phenotype Ontology associations
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     PRG4* Prg4* View 1 model HGNC
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
MGI 6.07
The Jackson Laboratory