{
    "disease_id": "DOID:0070191",
    "recommended_name": {
        "id": "DOID:0070191",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070191",
        "name": "autosomal recessive chronic granulomatous disease 2",
        "description": "A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF2 gene on chromosome 1q25."
    },
    "synonyms": [
        {
            "id": "DOID:0070191",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070191",
            "name": "CDG2",
            "description": ""
        },
        {
            "id": "DOID:0070191",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070191",
            "name": "deficiency of NCF2",
            "description": ""
        },
        {
            "id": "DOID:0070191",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070191",
            "name": "deficiency of p67-PHOX",
            "description": ""
        },
        {
            "id": "DOID:0070191",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070191",
            "name": "chronic granulomatous disease due to deficiency of NCF-2",
            "description": ""
        },
        {
            "id": "DOID:0070191",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070191",
            "name": "autosomal recessive chronic granulomatous disease cytochrome b-positive type II",
            "description": ""
        },
        {
            "id": "MONDO:0009310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009310",
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2",
            "description": "Any chronic granulomatous disease in which the cause of the disease is a mutation in the NCF2 gene."
        },
        {
            "id": "MONDO:0009310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009310",
            "name": "NCF2 chronic granulomatous disease",
            "description": ""
        },
        {
            "id": "MONDO:0009310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009310",
            "name": "chronic granulomatous disease 2, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009310",
            "name": "chronic granulomatous disease caused by mutation in NCF2",
            "description": ""
        },
        {
            "id": "MONDO:0009310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009310",
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009310",
            "name": "CDG2",
            "description": ""
        },
        {
            "id": "MIM:233710",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/233710",
            "name": "Granulomatous disease, chronic, autosomal recessive, 2",
            "description": "Granulomatous disease, chronic, autosomal recessive, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070191"
    ],
    "unlinked_id_list": []
}