{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "camptodactyly-arthropathy-coxa vara-pericarditis syndrome; CACP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "hypertrophic synovitis, congenital familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "fibrosing serositis, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "PAC syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "camptodactyly-arthropathy-coxa-vara-pericarditis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "camptodactyly-arthropathy-pericarditis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "familial fibrosing serositis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "arthropathy-camptodactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "pericarditis-arthropathy-camptodactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "congenital familial hypertrophic synovitis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "CACP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "Jacobs syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "CAP syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "camptodactyly arthropathy coxa vara pericarditis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "arthropathy camptodactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "pericarditis arthropathy camptodactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "camptodactyly arthropathy pericarditis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008828", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008828", 
            "name": "CACP syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "CACP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "CACP syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "CAP syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "Jacobs syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "PAC syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "arthropathy-camptodactyly syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "camptodactyly-arthropathy-pericarditis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "congenital familial hypertrophic synovitis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "familial fibrosing serositis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090127", 
            "name": "pericarditis-arthropathy-camptodactyly syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090127", 
        "description": "A syndrome that is characterized by congenital or early-onset camptodactyly, noninflammatory arthropathy with synovial hyperplasia and in some patients progressive coxa vara deformity, and/or noninflammatory pericardial or pleural effusion that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the proteoglycan 4 gene (PRG4) on chromosome 1q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090127", 
        "name": "camptodactyly-arthropathy-coxa vara-pericarditis syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/208250", 
            "id": "208250", 
            "database": "MIM"
        }
    ]
}