{
    "disease_id": "DOID:0111768",
    "recommended_name": {
        "id": "DOID:0111768",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111768",
        "name": "X-linked properdin deficiency",
        "description": "A complement deficiency characterized by decreased plasma levels of complement factor properdin and increased susceptibility to Neisseria species infections that has_material_basis_in homozygous or hemizygous mutation in PFC on chromosome Xp11.23."
    },
    "synonyms": [
        {
            "id": "DOID:0111768",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111768",
            "name": "CFPD",
            "description": ""
        },
        {
            "id": "DOID:0111768",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111768",
            "name": "complement factor properdin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010713",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010713",
            "name": "properdin deficiency, X-linked",
            "description": "A rare, hereditary, primary immunodeficiency due to a complement cascade protein anomaly characterized by significantly increased susceptibility to Neisseria species infections. It only affects males, typically presenting with severe or fulminant meningococcal disease."
        },
        {
            "id": "MONDO:0010713",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010713",
            "name": "properdin deficiency, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010713",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010713",
            "name": "properdin deficiency, X-linked, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010713",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010713",
            "name": "CFPD",
            "description": ""
        },
        {
            "id": "MONDO:0010713",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010713",
            "name": "PFD",
            "description": ""
        },
        {
            "id": "MIM:312060",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/312060",
            "name": "Properdin deficiency",
            "description": "Properdin deficiency"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111768"
    ],
    "unlinked_id_list": []
}