{
    "disease_id": "DOID:0111592",
    "recommended_name": {
        "id": "DOID:0111592",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111592",
        "name": "plasminogen deficiency type I",
        "description": "A syndrome characterized by decreased serum plasminogen activity, decreased plasminogen antigen levels, and chronic mucosal pseudomembranous lesions typically manifesting as ligneous conjunctivitis that has_material_basis_in homozygous or compound heterozygous mutation in PLG on chromosome 6q26."
    },
    "synonyms": [
        {
            "id": "DOID:0111592",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111592",
            "name": "hypoplasminogenemia",
            "description": ""
        },
        {
            "id": "MONDO:0009009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009009",
            "name": "hypoplasminogenemia",
            "description": "A rare multi-system disease characterized by markedly impaired extracellular fibrinolysis leading to the formation of ligneous (fibrin-rich) pseudomembranes on mucosae."
        },
        {
            "id": "MONDO:0009009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009009",
            "name": "hypoplasminogenemia",
            "description": ""
        },
        {
            "id": "MONDO:0009009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009009",
            "name": "plasminogen deficiency type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009009",
            "name": "plasminogen deficiency, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009009",
            "name": "plasminogen deficiency, type I",
            "description": ""
        },
        {
            "id": "MONDO:0009009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009009",
            "name": "type 1 plasminogen deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009009",
            "name": "ligneous conjunctivitis",
            "description": ""
        },
        {
            "id": "MIM:217090",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/217090",
            "name": "Plasminogen deficiency",
            "description": "Plasminogen deficiency"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111592"
    ],
    "unlinked_id_list": []
}