{
    "disease_id": "DOID:0060284",
    "recommended_name": {
        "id": "DOID:0060284",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060284",
        "name": "paroxysmal nocturnal hemoglobinuria",
        "description": "An acquired 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."
    },
    "synonyms": [
        {
            "id": "MONDO:0010438",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010438",
            "name": "paroxysmal nocturnal hemoglobinuria 1",
            "description": "Any paroxysmal nocturnal hemoglobinuria in which the cause of the disease is a mutation in the PIGA gene."
        },
        {
            "id": "MONDO:0010438",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010438",
            "name": "PIGA paroxysmal nocturnal hemoglobinuria",
            "description": ""
        },
        {
            "id": "MONDO:0010438",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010438",
            "name": "pIgA paroxysmal nocturnal hemoglobinuria",
            "description": ""
        },
        {
            "id": "MONDO:0010438",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010438",
            "name": "paroxysmal nocturnal hemoglobinuria 1",
            "description": ""
        },
        {
            "id": "MONDO:0010438",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010438",
            "name": "paroxysmal nocturnal hemoglobinuria caused by mutation in PIGA",
            "description": ""
        },
        {
            "id": "MONDO:0010438",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010438",
            "name": "paroxysmal nocturnal hemoglobinuria caused by mutation in pIgA",
            "description": ""
        },
        {
            "id": "MONDO:0010438",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010438",
            "name": "paroxysmal nocturnal hemoglobinuria type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010438",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010438",
            "name": "paroxysmal nocturnal hemoglobinuria, somatic",
            "description": ""
        },
        {
            "id": "MONDO:0010438",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010438",
            "name": "PNH1",
            "description": ""
        },
        {
            "id": "MONDO:0014166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014166",
            "name": "paroxysmal nocturnal hemoglobinuria 2",
            "description": "Any paroxysmal nocturnal hemoglobinuria in which the cause of the disease is a mutation in the PIGT gene."
        },
        {
            "id": "MONDO:0014166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014166",
            "name": "PIGT paroxysmal nocturnal hemoglobinuria",
            "description": ""
        },
        {
            "id": "MONDO:0014166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014166",
            "name": "paroxysmal nocturnal hemoglobinuria 2",
            "description": ""
        },
        {
            "id": "MONDO:0014166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014166",
            "name": "paroxysmal nocturnal hemoglobinuria 2, autosomal dominant, somatic mutation",
            "description": ""
        },
        {
            "id": "MONDO:0014166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014166",
            "name": "paroxysmal nocturnal hemoglobinuria caused by mutation in PIGT",
            "description": ""
        },
        {
            "id": "MONDO:0014166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014166",
            "name": "paroxysmal nocturnal hemoglobinuria type 2",
            "description": ""
        },
        {
            "id": "MONDO:0014166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014166",
            "name": "PNH2",
            "description": ""
        },
        {
            "id": "MIM:300818",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300818",
            "name": "Paroxysmal nocturnal hemoglobinuria 1",
            "description": "Paroxysmal nocturnal hemoglobinuria 1"
        },
        {
            "id": "MIM:615399",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615399",
            "name": "Paroxysmal nocturnal hemoglobinuria 2",
            "description": "Paroxysmal nocturnal hemoglobinuria 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060284"
    ],
    "unlinked_id_list": []
}