{
    "disease_id": "DOID:0061004",
    "recommended_name": {
        "id": "DOID:0061004",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061004",
        "name": "poor metabolism of thiopurines 1",
        "description": "A poor metabolism of thiopurines that has_material_basis_in homozygous or compound heterozygous mutation in the TPMT gene on chromosome 6p22."
    },
    "synonyms": [
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "thiopurine S-methyltransferase deficiency",
            "description": "An inherited metabolic disease that is has its basis in the disruption of thiopurine S-methyltransferase activity."
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "TPMT deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "inborn error of thiopurine S-methyltransferase activity",
            "description": ""
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "inborn thiopurine S-methyltransferase activity disorder",
            "description": ""
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "poor metabolism of thiopurines-1",
            "description": ""
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "rare inborn error of thiopurine S-methyltransferase activity",
            "description": ""
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "thiopurine S-methyltransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "6-mercaptopurine sensitivity",
            "description": ""
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "THPM1",
            "description": ""
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "thiopurine S methyltranferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012503",
            "name": "thiopurine methyltransferase deficiency",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061004"
    ],
    "unlinked_id_list": []
}