{
    "disease_id": "DOID:8158", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012295", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012295", 
            "name": "complement component 5 deficiency; C5D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012295", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012295", 
            "name": "C5D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012295", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012295", 
            "name": "complement deficiency caused by mutation in C5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012295", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012295", 
            "name": "dysfunction of the fifth component of complement (C5)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012295", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012295", 
            "name": "C5 complement deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012295", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012295", 
            "name": "C5 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:8158", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:8158", 
            "name": "C5 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:8158", 
        "description": "A complement deficiency that is characterized by susceptibility to recurrent bacterial infections especially to infections of enveloped organisms, and has_material_basis_in mutation in the complement component 5 (C5) gene on chromosome 9q33.2 that encodes the fifth component of complenent, a part of the innate immune system.", 
        "resource": "Disease Ontology", 
        "id": "DOID:8158", 
        "name": "complement component 5 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/609536", 
            "id": "609536", 
            "database": "MIM"
        }
    ]
}