{
    "disease_id": "DOID:0080621",
    "recommended_name": {
        "id": "DOID:0080621",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080621",
        "name": "glucocorticoid deficiency 1",
        "description": "A familial glucocorticoid deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding melanocortin-2 receptor, which is also referred to as adrenocorticotropin receptor, on chromosome 18p11."
    },
    "synonyms": [
        {
            "id": "MONDO:0024536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024536",
            "name": "glucocorticoid deficiency 1",
            "description": "Any familial glucocorticoid deficiency in which the cause of the disease is a mutation in the MC2R gene."
        },
        {
            "id": "MONDO:0024536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024536",
            "name": "MC2R familial glucocorticoid deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0024536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024536",
            "name": "familial glucocorticoid deficiency caused by mutation in MC2R",
            "description": ""
        },
        {
            "id": "MONDO:0024536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024536",
            "name": "glucocorticoid deficiency 1",
            "description": ""
        },
        {
            "id": "MONDO:0024536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024536",
            "name": "glucocorticoid deficiency, due to ACTH unresponsiveness",
            "description": ""
        },
        {
            "id": "MONDO:0024536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024536",
            "name": "GCCD1",
            "description": ""
        },
        {
            "id": "MIM:202200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/202200",
            "name": "Glucocorticoid deficiency 1",
            "description": "Glucocorticoid deficiency 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080621"
    ],
    "unlinked_id_list": []
}