{
    "disease_id": "DOID:0050718",
    "recommended_name": {
        "id": "DOID:0050718",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050718",
        "name": "vitamin metabolic disorder",
        "description": "An inherited metabolic disorder resulting from a deficiency in vitamin or vitamin cofactor transport or metabolism."
    },
    "synonyms": [],
    "children": [
        {
            "id": "DOID:0050719",
            "label": "cerebral folate receptor alpha deficiency",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050731",
            "label": "vitamin B12 deficiency",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0050734",
                    "label": "congenital intrinsic factor deficiency",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050818",
                    "label": "transcobalamin II deficiency",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0061185",
            "label": "autoinflammatory syndrome with cytopenia, hyperzincemia, and hypercalprotectinemia",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070742",
            "label": "combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0090028",
            "label": "familial isolated deficiency of vitamin E",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111329",
            "label": "pyridoxamine 5'-phosphate oxidase deficiency",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111678",
            "label": "hereditary folate malabsorption",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111679",
            "label": "glutamate formiminotransferase deficiency",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070742",
        "DOID:0061185",
        "DOID:0050718",
        "DOID:0111679",
        "DOID:0111678",
        "DOID:0111329",
        "DOID:0050734",
        "DOID:0050731",
        "DOID:0090028",
        "DOID:0050818",
        "DOID:0050719"
    ],
    "unlinked_id_list": []
}