{
    "disease_id": "DOID:0090127",
    "recommended_name": {
        "id": "DOID:0090127",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0090127",
        "name": "camptodactyly-arthropathy-coxa vara-pericarditis syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "CACP",
            "description": ""
        },
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "CACP syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "CAP syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "Jacobs syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "PAC syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "arthropathy-camptodactyly syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "camptodactyly-arthropathy-pericarditis syndrome",
            "description": ""
        },
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "congenital familial hypertrophic synovitis",
            "description": ""
        },
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "familial fibrosing serositis",
            "description": ""
        },
        {
            "id": "DOID:0090127",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090127",
            "name": "pericarditis-arthropathy-camptodactyly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "camptodactyly-arthropathy-coxa vara-pericarditis syndrome",
            "description": "Camptodactyly-arthropathy-coxa-vara-pericarditis (CACP) syndrome is a rare, genetic, rheumatologic disease characterized by congenital or early-onset camptodactyly and symmetrical, polyarticular, non-inflammatory, large joint arthropathy with synovial hyperplasia, as well as progressive coxa vara deformity and, occasionally, non-inflammatory pericarditis."
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "CACP",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "CACP syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "Jacobs syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "PAC syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "arthropathy-camptodactyly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "camptodactyly-arthropathy-coxa vara-pericarditis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "camptodactyly-arthropathy-pericarditis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "pericarditis-arthropathy-camptodactyly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "arthropathy camptodactyly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "camptodactyly arthropathy coxa vara pericarditis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "camptodactyly arthropathy pericarditis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "camptodactyly-arthropathy-coxa-vara-pericarditis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "fibrosing serositis, familial",
            "description": ""
        },
        {
            "id": "MONDO:0008828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008828",
            "name": "pericarditis arthropathy camptodactyly syndrome",
            "description": ""
        },
        {
            "id": "MIM:208250",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/208250",
            "name": "Camptodactyly-arthropathy-coxa vara-pericarditis syndrome",
            "description": "Camptodactyly-arthropathy-coxa vara-pericarditis syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0090127"
    ],
    "unlinked_id_list": []
}