{
    "disease_id": "DOID:0111592", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009009", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009009", 
            "name": "hypoplasminogenemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009009", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009009", 
            "name": "plasminogen deficiency, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009009", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009009", 
            "name": "ligneous conjunctivitis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009009", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009009", 
            "name": "type 1 plasminogen deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009009", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009009", 
            "name": "Dysplasminogenemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009009", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009009", 
            "name": "plasminogen deficiency, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009009", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009009", 
            "name": "plasminogen deficiency, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009009", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009009", 
            "name": "plasminogen deficiency type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111592", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111592", 
            "name": "hypoplasminogenemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111592", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111592", 
        "name": "plasminogen deficiency type I"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111592#disease-associations", 
            "id": "0111592", 
            "database": "Alliance of Genome Resources"
        }
    ]
}