{
    "disease_id": "DOID:0061020",
    "recommended_name": {
        "id": "DOID:0061020",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061020",
        "name": "combined pituitary hormone deficiency 2",
        "description": "A combined pituitary hormone deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the PROP1 gene on chromosome 5q35."
    },
    "synonyms": [
        {
            "id": "DOID:0061020",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061020",
            "name": "CPHD2",
            "description": ""
        },
        {
            "id": "MONDO:0009878",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009878",
            "name": "pituitary hormone deficiency, combined, 2",
            "description": "Any combined pituitary hormone deficiencies, genetic form in which the cause of the disease is a mutation in the PROP1 gene."
        },
        {
            "id": "MONDO:0009878",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009878",
            "name": "PROP1 combined pituitary hormone deficiencies, genetic form",
            "description": ""
        },
        {
            "id": "MONDO:0009878",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009878",
            "name": "combined pituitary hormone deficiencies, genetic form caused by mutation in PROP1",
            "description": ""
        },
        {
            "id": "MONDO:0009878",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009878",
            "name": "pituitary hormone deficiency, combined, 2",
            "description": ""
        },
        {
            "id": "MONDO:0009878",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009878",
            "name": "pituitary hormone deficiency, combined, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009878",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009878",
            "name": "CPHD2",
            "description": ""
        },
        {
            "id": "MIM:262600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/262600",
            "name": "Pituitary hormone deficiency, combined, 2",
            "description": "Pituitary hormone deficiency, combined, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061020"
    ],
    "unlinked_id_list": []
}