{
    "disease_id": "DOID:0112125",
    "recommended_name": {
        "id": "DOID:0112125",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112125",
        "name": "alpha-thalassemia myelodysplasia syndrome",
        "description": "A syndrome characterized by acquired alpha-thalassemia in association with a multilineage myelodysplasia that has_material_basis_in somatic mutation in the ATRX gene on chromosome Xq21.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112125",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112125",
            "name": "ATMDS",
            "description": ""
        },
        {
            "id": "DOID:0112125",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112125",
            "name": "acquired HbH disease",
            "description": ""
        },
        {
            "id": "DOID:0112125",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112125",
            "name": "acquired hemoglobin H disease",
            "description": ""
        },
        {
            "id": "DOID:0112125",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112125",
            "name": "alpha-thalassemia-myelodysplastic syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010328",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010328",
            "name": "alpha-thalassemia-myelodysplastic syndrome",
            "description": "Alpha-thalassemia-myelodysplastic syndrome (ATMDS) is an acquired form of alpha-thalassemia characterized by a myelodysplastic syndrome (MDS) or more rarely a myeloproliferative disease (MPD) associated with hemoglobin H disease (HbH)."
        },
        {
            "id": "MONDO:0010328",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010328",
            "name": "ATMDS",
            "description": ""
        },
        {
            "id": "MONDO:0010328",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010328",
            "name": "acquired HbH disease",
            "description": ""
        },
        {
            "id": "MONDO:0010328",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010328",
            "name": "acquired haemoglobin H disease",
            "description": ""
        },
        {
            "id": "MONDO:0010328",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010328",
            "name": "acquired hemoglobin H disease",
            "description": ""
        },
        {
            "id": "MONDO:0010328",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010328",
            "name": "alpha-thalassemia myelodysplasia syndrome, somatic",
            "description": ""
        },
        {
            "id": "MONDO:0010328",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010328",
            "name": "ALPHA-thalassemia myelodysplasia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010328",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010328",
            "name": "Haemoglobin H disease, acquired",
            "description": ""
        },
        {
            "id": "MIM:300448",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300448",
            "name": "Alpha-thalassemia myelodysplasia syndrome",
            "description": "Alpha-thalassemia myelodysplasia syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112125"
    ],
    "unlinked_id_list": []
}