{
    "disease_id": "DOID:0080626",
    "recommended_name": {
        "id": "DOID:0080626",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080626",
        "name": "corticosterone methyloxidase deficiency 1",
        "description": "An adrenal gland disease that is characterized by excessive amounts of sodium released in the urine, along with insufficient release of potassium in the urine, usually beginning in the first few weeks of life."
    },
    "synonyms": [
        {
            "id": "DOID:0080626",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080626",
            "name": "aldosterone synthase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008751",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008751",
            "name": "corticosterone methyloxidase type 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008751",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008751",
            "name": "corticosterone 18-monooxygenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008751",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008751",
            "name": "corticosterone methyloxidase type 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008751",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008751",
            "name": "hypoaldosteronism, congenital, due to cmo i deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008751",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008751",
            "name": "18 Hydroxylase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008751",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008751",
            "name": "18 alpha hydroxylase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008751",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008751",
            "name": "CMO 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008751",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008751",
            "name": "aldosterone deficiency 1",
            "description": ""
        },
        {
            "id": "MONDO:0008751",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008751",
            "name": "aldosterone deficiency due to defect in 18 hydroxylase",
            "description": ""
        },
        {
            "id": "MIM:203400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/203400",
            "name": "Corticosterone methyloxidase 1 deficiency",
            "description": "Corticosterone methyloxidase 1 deficiency"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080626"
    ],
    "unlinked_id_list": []
}