{
    "disease_id": "DOID:1156", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:1156", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1156", 
            "name": "pseudogout"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1156", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1156", 
            "name": "calcium pyrophosphate deposition disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "Familial calcium pyrophosphate deposition (CPPD) is a chronic inherited arthropathy characterized by chondrocalcinosis (CC; i.e. cartilage calcification), often associated with recurrent acute calcium pyrophosphate (CPP) crystal arthritis and polyarticular osteoarthritis (OA).", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "familial calcium pyrophosphate deposition"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "chondrocalcinosis 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "chondrocalcinosis 2; CCAL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "hereditary CC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "hereditary articular chondrocalcinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "familial CC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "calcium pyrophosphate arthropathy, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "calcium gout"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "chondrocalcinosis, familial articular"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "familial calcium pyrophosphate dihydrate deposition disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "hereditary calcium pyrophosphate deposition"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "familial articular chondrocalcinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "calcium pyrophosphate arthropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "Pseudogout, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "familial CPPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "CCAL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "calcium pyrophosphate dihydrate deposition disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "chondrocalcinosis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "calcium pyrophosphate dihydrate crystal deposition disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "CPPDD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "calcium gout, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007319", 
            "name": "chondrocalcinosis familial articular"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010917", 
            "name": "CCAL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010917", 
            "name": "chondrocalcinosis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010917", 
            "name": "CCAL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010917", 
            "name": "chondrocalcinosis 1; CCAL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010917", 
            "name": "chondrocalcinosis with early-onset osteoarthritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007320", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007320", 
            "name": "chondrocalcinosis due to apatite crystal deposition"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007320", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007320", 
            "name": "chondrocalcinosis due to apatite crystal deposition"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007320", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007320", 
            "name": "familial apatite disease"
        }, 
        {
            "url": "https://www.omim.org/entry/118600", 
            "description": "Chondrocalcinosis 2", 
            "resource": "MIM", 
            "id": "MIM:118600", 
            "name": "Chondrocalcinosis 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1156", 
        "description": "An arthritis that has_material_basis_in the accumulation of salt crystals located_in joint.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1156", 
        "name": "chondrocalcinosis"
    }
}