{
    "disease_id": "DOID:0110918",
    "recommended_name": {
        "id": "DOID:0110918",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110918",
        "name": "hereditary spherocytosis type 3",
        "description": "A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110918",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110918",
            "name": "HS3",
            "description": ""
        },
        {
            "id": "DOID:0110918",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110918",
            "name": "SPH3",
            "description": ""
        },
        {
            "id": "DOID:0110918",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110918",
            "name": "hereditary spherocytosis 3",
            "description": ""
        },
        {
            "id": "MONDO:0010053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010053",
            "name": "hereditary spherocytosis type 3",
            "description": "Any hereditary spherocytosis in which the cause of the disease is a mutation in the SPTA1 gene."
        },
        {
            "id": "MONDO:0010053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010053",
            "name": "HS3",
            "description": ""
        },
        {
            "id": "MONDO:0010053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010053",
            "name": "SPH3",
            "description": ""
        },
        {
            "id": "MONDO:0010053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010053",
            "name": "SPTA1 hereditary spherocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0010053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010053",
            "name": "hereditary spherocytosis caused by mutation in SPTA1",
            "description": ""
        },
        {
            "id": "MONDO:0010053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010053",
            "name": "spherocytosis, type 3",
            "description": ""
        },
        {
            "id": "MIM:270970",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/270970",
            "name": "Spherocytosis 3",
            "description": "Spherocytosis 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110918"
    ],
    "unlinked_id_list": []
}