{
    "disease_id": "DOID:0060301",
    "recommended_name": {
        "id": "DOID:0060301",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060301",
        "name": "type I complement component 8 deficiency",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "type I complement component 8 deficiency",
            "description": "Any classic complement early component deficiency in which the cause of the disease is a mutation in the C8A gene."
        },
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "C8 deficiency, type I",
            "description": ""
        },
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "C8A classic complement early component deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "classic complement early component deficiency caused by mutation in C8A",
            "description": ""
        },
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "C8 deficiency type I",
            "description": ""
        },
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "C81 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "C8D1",
            "description": ""
        },
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "complement component 8 deficiency type 1",
            "description": ""
        },
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "complement component 8 deficiency type I",
            "description": ""
        },
        {
            "id": "MONDO:0013422",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013422",
            "name": "complement component 8 deficiency, type I",
            "description": ""
        },
        {
            "id": "MIM:613790",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613790",
            "name": "Complement component 8 deficiency, 1",
            "description": "Complement component 8 deficiency, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060301"
    ],
    "unlinked_id_list": []
}