{
    "disease_id": "DOID:0061249",
    "recommended_name": {
        "id": "DOID:0061249",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061249",
        "name": "familial hyperaldosteronism II",
        "description": "A familial hyperaldosteronism characterized by hypertension due to increased aldosterone, often with hypokalemia that has_material_basis_in heterozygous mutation in the CLCN2 gene on chromosome 3q27."
    },
    "synonyms": [
        {
            "id": "MONDO:0011576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011576",
            "name": "familial hyperaldosteronism type II",
            "description": "Familial hyperaldosteronism type II (FH-II) is a heritable form of primary aldosteronism (PA) characterized by hypertension of varying severity, and non glucocticoid remediable hyperaldosteronism."
        },
        {
            "id": "MONDO:0011576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011576",
            "name": "FH-II",
            "description": ""
        },
        {
            "id": "MONDO:0011576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011576",
            "name": "FH2",
            "description": ""
        },
        {
            "id": "MONDO:0011576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011576",
            "name": "familial adrenal adenoma",
            "description": ""
        },
        {
            "id": "MONDO:0011576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011576",
            "name": "familial hyperaldosteronism type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011576",
            "name": "FHII",
            "description": ""
        },
        {
            "id": "MONDO:0011576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011576",
            "name": "HALD2",
            "description": ""
        },
        {
            "id": "MIM:605635",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/605635",
            "name": "Hyperaldosteronism, familial, 2",
            "description": "Hyperaldosteronism, familial, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061249"
    ],
    "unlinked_id_list": []
}