{
    "disease_id": "DOID:0060284", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014166", 
            "name": "paroxysmal nocturnal hemoglobinuria 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014166", 
            "name": "paroxysmal nocturnal hemoglobinuria caused by mutation in PIGT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014166", 
            "name": "PIGT paroxysmal nocturnal hemoglobinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014166", 
            "name": "PNH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014166", 
            "name": "paroxysmal nocturnal hemoglobinuria 2; PNH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014166", 
            "name": "paroxysmal nocturnal hemoglobinuria type 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060284", 
        "description": "An aquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060284", 
        "name": "paroxysmal nocturnal hemoglobinuria"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060284#disease-associations", 
            "id": "0060284", 
            "database": "Alliance of Genome Resources"
        }
    ]
}