{
    "disease_id": "DOID:0070193",
    "recommended_name": {
        "id": "DOID:0070193",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070193",
        "name": "autosomal recessive chronic granulomatous disease cytochrome b-negative",
        "description": "A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the CYBA gene on chromosome 16q24.2."
    },
    "synonyms": [
        {
            "id": "DOID:0070193",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070193",
            "name": "CYBA deficiency",
            "description": ""
        },
        {
            "id": "DOID:0070193",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070193",
            "name": "CGD due to deficiency of the alpha subunit of cytochrome b",
            "description": ""
        },
        {
            "id": "DOID:0070193",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070193",
            "name": "autosomal recessive cytochrome b-negative CGD",
            "description": ""
        },
        {
            "id": "DOID:0070193",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070193",
            "name": "chronic granulomatous disease due to deficiency of CYBA",
            "description": ""
        },
        {
            "id": "DOID:0070193",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070193",
            "name": "autosomal recessive chronic granulomatous disease 4",
            "description": ""
        },
        {
            "id": "MONDO:0009308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009308",
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-negative",
            "description": ""
        },
        {
            "id": "MONDO:0009308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009308",
            "name": "Cyba deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009308",
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-negative",
            "description": ""
        },
        {
            "id": "MONDO:0009308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009308",
            "name": "CGD, autosomal recessive cytochrome B-negative",
            "description": ""
        },
        {
            "id": "MONDO:0009308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009308",
            "name": "CGD due to deficiency of the Alpha Subunit of cytochrome B",
            "description": ""
        },
        {
            "id": "MIM:233690",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/233690",
            "name": "Granulomatous disease, chronic, autosomal recessive, 4",
            "description": "Granulomatous disease, chronic, autosomal recessive, 4"
        }
    ]
}