{
    "disease_id": "DOID:0070194",
    "recommended_name": {
        "id": "DOID:0070194",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070194",
        "name": "autosomal recessive chronic granulomatous disease 3",
        "description": "A chronic granulomatous disease characterized by that autosomal recessive inheritance has_material_basis_in mutation in the NCF4 gene on chromosome 22q12."
    },
    "synonyms": [
        {
            "id": "DOID:0070194",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070194",
            "name": "autosomal recessive cytochrome b-positive CGD type III",
            "description": ""
        },
        {
            "id": "DOID:0070194",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070194",
            "name": "CDG3",
            "description": ""
        },
        {
            "id": "DOID:0070194",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070194",
            "name": "chronic granulomatous disease due to NCF4 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0070194",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070194",
            "name": "autosomal recessive chronic granulomatous disease cytochrome b-positive type III",
            "description": ""
        },
        {
            "id": "MONDO:0013507",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013507",
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0013507",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013507",
            "name": "chronic granulomatous disease 3, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0013507",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013507",
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0013507",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013507",
            "name": "CDG3",
            "description": ""
        },
        {
            "id": "MIM:613960",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613960",
            "name": "Granulomatous disease, chronic, autosomal recessive, 3",
            "description": "Granulomatous disease, chronic, autosomal recessive, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070194"
    ],
    "unlinked_id_list": []
}