{
    "disease_id": "DOID:0070194", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013507", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013507", 
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013507", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013507", 
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type III; CDG3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013507", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013507", 
            "name": "granulomatous disease, chronic, due to Ncf4 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013507", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013507", 
            "name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013507", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013507", 
            "name": "CGD, autosomal recessive cytochrome B-positive, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013507", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013507", 
            "name": "CDG3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070194", 
            "name": "autosomal recessive cytochrome b-positive CGD type III"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070194", 
            "name": "CDG3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070194", 
            "name": "chronic granulomatous disease due to NCF4 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070194", 
            "name": "autosomal recessive chronic granulomatous disease 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070194", 
        "description": "A chronic granulomatous disease characterized by that autosomal recessive inheritance has_material_basis_in mutation in the NCF4 gene on chromosome 22q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070194", 
        "name": "autosomal recessive chronic granulomatous disease cytochrome b-positive type III"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070194#disease-associations", 
            "id": "0070194", 
            "database": "Alliance of Genome Resources"
        }
    ]
}