{
    "disease_id": "DOID:0060302", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "classic complement early component deficiency caused by mutation in C8B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "Human complement C8-beta deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "C8 deficiency, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "complement component 8B deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "complement component 8 deficiency type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "complement component 8 deficiency, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "C8 Beta deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "C8D2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "complement component 8 deficiency, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "complement component 8 deficiency, type II; C8D2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "C8B deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "C8B classic complement early component deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "complement component 8 deficiency type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013421", 
            "name": "C8 deficiency type II"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060302", 
        "description": "A complement deficiency that is characterized by deficiency of the beta subunit of complement protein 8, which causes increased susceptibility to recurrent bacterial infections, especially to Neisseria meningitidis, and has_material_basis_in autosomal recessive inheritance of mutation in the C8B gene, which produces the beta subunit of complement component 8 important in forming membrane attack complexes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060302", 
        "name": "type II complement component 8 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060302#disease-associations", 
            "id": "0060302", 
            "database": "Alliance of Genome Resources"
        }
    ]
}