{
    "disease_id": "DOID:0110923",
    "recommended_name": {
        "id": "DOID:0110923",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110923",
        "name": "familial hemophagocytic lymphohistiocytosis 3",
        "description": "A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the UNC13D gene on chromosome 17q25.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110923",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110923",
            "name": "FHL3",
            "description": ""
        },
        {
            "id": "DOID:0110923",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110923",
            "name": "HLH3",
            "description": ""
        },
        {
            "id": "DOID:0110923",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110923",
            "name": "HPLH3",
            "description": ""
        },
        {
            "id": "MONDO:0012146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012146",
            "name": "familial hemophagocytic lymphohistiocytosis 3",
            "description": "Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the UNC13D gene."
        },
        {
            "id": "MONDO:0012146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012146",
            "name": "FHL3",
            "description": ""
        },
        {
            "id": "MONDO:0012146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012146",
            "name": "HLH3",
            "description": ""
        },
        {
            "id": "MONDO:0012146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012146",
            "name": "HPLH3",
            "description": ""
        },
        {
            "id": "MONDO:0012146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012146",
            "name": "UNC13D genetic hemophagocytic lymphohistiocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0012146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012146",
            "name": "familial hemophagocytic lymphohistiocytosis type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012146",
            "name": "genetic hemophagocytic lymphohistiocytosis caused by mutation in UNC13D",
            "description": ""
        },
        {
            "id": "MONDO:0012146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012146",
            "name": "hemophagocytic lymphohistiocytosis, familial, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012146",
            "name": "hemophagocytic lymphohistiocytosis, familial, 3",
            "description": ""
        },
        {
            "id": "MIM:608898",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608898",
            "name": "Hemophagocytic lymphohistiocytosis, familial, 3",
            "description": "Hemophagocytic lymphohistiocytosis, familial, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110923"
    ],
    "unlinked_id_list": []
}