{
    "disease_id": "DOID:0061018",
    "recommended_name": {
        "id": "DOID:0061018",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061018",
        "name": "combined or isolated pituitary hormone deficiency 8",
        "description": "A combined pituitary hormone deficiency that has_material_basis_in heterozygous mutation in the ROBO1 gene on chromosome 3p12."
    },
    "synonyms": [
        {
            "id": "DOID:0061018",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061018",
            "name": "CPHD8",
            "description": ""
        },
        {
            "id": "MONDO:0957208",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957208",
            "name": "pituitary hormone deficiency, combined or isolated, 8",
            "description": ""
        },
        {
            "id": "MIM:620303",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620303",
            "name": "Pituitary hormone deficiency, combined or isolated, 8",
            "description": "Pituitary hormone deficiency, combined or isolated, 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061018"
    ],
    "unlinked_id_list": []
}