{
    "disease_id": "DOID:0060301", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "classic complement early component deficiency caused by mutation in C8A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "complement component 8 deficiency type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "C8 deficiency, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "C8 deficiency type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "complement component 8 deficiency, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "C8A classic complement early component deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "C81 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "C8Ag deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "complement component 8 deficiency type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "complement component 8 deficiency, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "C8D1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "C8 Alpha-gamma deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013422", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013422", 
            "name": "complement component 8 deficiency, type I; C8D1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060301", 
        "description": "A complement deficiency that is characterized by deficiency of the alpha 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 C8A gene, which produces the alpha subunit of complement component 8 important in forming membrane attack complexes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060301", 
        "name": "type I complement component 8 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060301#disease-associations", 
            "id": "0060301", 
            "database": "Alliance of Genome Resources"
        }
    ]
}