{
    "disease_id": "DOID:0061026",
    "recommended_name": {
        "id": "DOID:0061026",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061026",
        "name": "hereditary pyropoikilocytosis",
        "description": "A hemolytic anemia characterized by microspherocytosis, poikilocytosis, and an unusual thermal sensitivity of red cells that has_material_basis_in mutation in the alpha-spectrin or the beta-spectrin gene."
    },
    "synonyms": [
        {
            "id": "DOID:0061026",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061026",
            "name": "HPP",
            "description": ""
        },
        {
            "id": "MONDO:0009948",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009948",
            "name": "pyropoikilocytosis, hereditary",
            "description": "An autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency."
        },
        {
            "id": "MONDO:0009948",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009948",
            "name": "Hypophosphatasia",
            "description": ""
        },
        {
            "id": "MONDO:0009948",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009948",
            "name": "pyropoikilocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0009948",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009948",
            "name": "pyropoikilocytosis, hereditary",
            "description": ""
        },
        {
            "id": "MONDO:0009948",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009948",
            "name": "HPP",
            "description": ""
        },
        {
            "id": "MONDO:0009948",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009948",
            "name": "hereditary pyropoikilocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0009948",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009948",
            "name": "pyropoikilocytosis hereditary",
            "description": ""
        },
        {
            "id": "MIM:266140",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/266140",
            "name": "Hereditary pyropoikilocytosis",
            "description": "Hereditary pyropoikilocytosis"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061026"
    ],
    "unlinked_id_list": []
}