{
    "disease_id": "DOID:0110920",
    "recommended_name": {
        "id": "DOID:0110920",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110920",
        "name": "hereditary spherocytosis type 5",
        "description": "A hereditary spherocytosis that has_material_basis_in a mutation of the EPB42 gene on chromosome 15q15.2."
    },
    "synonyms": [
        {
            "id": "DOID:0110920",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110920",
            "name": "HS5",
            "description": ""
        },
        {
            "id": "DOID:0110920",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110920",
            "name": "SPH5",
            "description": ""
        },
        {
            "id": "DOID:0110920",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110920",
            "name": "hereditary spherocytosis 5",
            "description": ""
        },
        {
            "id": "MONDO:0012985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012985",
            "name": "hereditary spherocytosis type 5",
            "description": "Any hereditary spherocytosis in which the cause of the disease is a mutation in the EPB42 gene."
        },
        {
            "id": "MONDO:0012985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012985",
            "name": "EPB42 hereditary spherocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0012985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012985",
            "name": "HS5",
            "description": ""
        },
        {
            "id": "MONDO:0012985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012985",
            "name": "SPH5",
            "description": ""
        },
        {
            "id": "MONDO:0012985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012985",
            "name": "hereditary spherocytosis caused by mutation in EPB42",
            "description": ""
        },
        {
            "id": "MONDO:0012985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012985",
            "name": "hereditary spherocytosis type 5",
            "description": ""
        },
        {
            "id": "MONDO:0012985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012985",
            "name": "spherocytosis, type 5",
            "description": ""
        },
        {
            "id": "MIM:612690",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612690",
            "name": "Spherocytosis 5",
            "description": "Spherocytosis 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110920"
    ],
    "unlinked_id_list": []
}