{
    "disease_id": "DOID:0070549",
    "recommended_name": {
        "id": "DOID:0070549",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070549",
        "name": "primary pigmented nodular adrenocortical disease 4",
        "description": "A primary pigmented nodular adrenocortical disease that has_material_basis_in duplication on chromosome 19p13 that includes the PRKACA gene."
    },
    "synonyms": [
        {
            "id": "DOID:0070549",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070549",
            "name": "PPNAD4",
            "description": ""
        },
        {
            "id": "DOID:0070549",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070549",
            "name": "chromosome 19p13 duplication syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014359",
            "name": "pigmented nodular adrenocortical disease, primary, 4",
            "description": "Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PRKACA gene."
        },
        {
            "id": "MONDO:0014359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014359",
            "name": "Cushing syndrome, ACTH-independent adrenal, somatic",
            "description": ""
        },
        {
            "id": "MONDO:0014359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014359",
            "name": "PRKACA primary pigmented nodular adrenocortical disease",
            "description": ""
        },
        {
            "id": "MONDO:0014359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014359",
            "name": "pigmented nodular adrenocortical disease, primary, 4",
            "description": ""
        },
        {
            "id": "MONDO:0014359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014359",
            "name": "pigmented nodular adrenocortical disease, primary, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0014359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014359",
            "name": "primary pigmented nodular adrenocortical disease caused by mutation in PRKACA",
            "description": ""
        },
        {
            "id": "MONDO:0014359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014359",
            "name": "PPNAD4",
            "description": ""
        },
        {
            "id": "MIM:615830",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615830",
            "name": "Primary pigmented nodular adrenocortical disease 4",
            "description": "Primary pigmented nodular adrenocortical disease 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070549"
    ],
    "unlinked_id_list": []
}