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