{
    "disease_id": "DOID:14283",
    "recommended_name": {
        "id": "DOID:14283",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14283",
        "name": "primary hypertrophic osteoarthropathy",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:14283",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14283",
            "name": "Pachydermoperiostosis of nail",
            "description": ""
        },
        {
            "id": "DOID:14283",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14283",
            "name": "Pachydermoperiostosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "hypertrophic osteoarthropathy, primary, autosomal recessive, 1",
            "description": "Any primary hypertrophic osteoarthropathy in which the cause of the disease is a mutation in the HPGD gene."
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "HPGD primary hypertrophic osteoarthropathy",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "Cranioosteoarthropathy",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "pachydermoperiostosis, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "PHOAR1",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "familial idiopathic osteoarthropathy of childhood",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "Touraine-Solente-Gole syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "Pho, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "primary hypertrophic osteoarthropathy caused by mutation in HPGD",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "PDP, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "Currarino idiopathic osteoarthropathy",
            "description": ""
        },
        {
            "id": "MONDO:0024546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024546",
            "name": "hypertrophic osteoarthropathy, primary, autosomal recessive, 1; PHOAR1",
            "description": ""
        },
        {
            "id": "MIM:259100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/259100",
            "name": "Cranioosteoarthropathy",
            "description": "Cranioosteoarthropathy"
        }
    ]
}