{
    "disease_id": "DOID:0061250",
    "recommended_name": {
        "id": "DOID:0061250",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061250",
        "name": "familial hyperaldosteronism IV",
        "description": "A familial hyperaldosteronism that has_material_basis_in heterozygous mutation in the CACNA1H gene on chromosome 16p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0014875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014875",
            "name": "hyperaldosteronism, familial, type IV",
            "description": ""
        },
        {
            "id": "MONDO:0014875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014875",
            "name": "HALD4",
            "description": ""
        },
        {
            "id": "MONDO:0014875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014875",
            "name": "familial hyperaldosteronism type IV",
            "description": ""
        },
        {
            "id": "MONDO:0014875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014875",
            "name": "hyperaldosteronism, familial, type IV",
            "description": ""
        },
        {
            "id": "MONDO:0014875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014875",
            "name": "hyperaldosteronism, familial, type IV; HALD4",
            "description": ""
        },
        {
            "id": "MIM:617027",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617027",
            "name": "Hyperaldosteronism, familial, 4",
            "description": "Hyperaldosteronism, familial, 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061250"
    ],
    "unlinked_id_list": []
}