{
    "disease_id": "DOID:0070192",
    "recommended_name": {
        "id": "DOID:0070192",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070192",
        "name": "autosomal recessive chronic granulomatous disease 1",
        "description": "A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF1 gene on chromosome 7q11.23."
    },
    "synonyms": [
        {
            "id": "DOID:0070192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070192",
            "name": "autosomal recessive chronic granulomatous disease cytochrome b-positive type I",
            "description": ""
        },
        {
            "id": "DOID:0070192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070192",
            "name": "CDG1",
            "description": ""
        },
        {
            "id": "DOID:0070192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070192",
            "name": "deficiency of NCF1",
            "description": ""
        },
        {
            "id": "DOID:0070192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070192",
            "name": "deficiency of SOC2",
            "description": ""
        },
        {
            "id": "DOID:0070192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070192",
            "name": "deficiency of neutrophil cytosol factor 1",
            "description": ""
        },
        {
            "id": "DOID:0070192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070192",
            "name": "deficiency of p47-PHOX",
            "description": ""
        },
        {
            "id": "DOID:0070192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070192",
            "name": "deficiency of soluble oxidase component II",
            "description": ""
        },
        {
            "id": "DOID:0070192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070192",
            "name": "chronic granulomatous disease due to deficiency of NCF-1",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1",
            "description": "Any chronic granulomatous disease in which the cause of the disease is a mutation in the NCF1 gene."
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "NCF1 chronic granulomatous disease",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "chronic granulomatous disease 1, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "chronic granulomatous disease caused by mutation in NCF1",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "CDG1",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "CGD, autosomal recessive cytochrome B-positive, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "Ncf1, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "Soc2, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type I",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "granulomatous disease, chronic, due to Ncf1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "neutrophil cytosol Factor 1, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "p47-PHOX, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0009309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009309",
            "name": "soluble oxidase component II, deficiency of",
            "description": ""
        },
        {
            "id": "MIM:233700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/233700",
            "name": "Granulomatous disease, chronic, autosomal recessive, 1",
            "description": "Granulomatous disease, chronic, autosomal recessive, 1"
        }
    ]
}