{
    "disease_id": "DOID:0110029",
    "recommended_name": {
        "id": "DOID:0110029",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110029",
        "name": "alpha thalassemia-intellectual disability syndrome type 1",
        "description": "An alpha thalassemia that has_material_basis_in a deletion in chromosome 16p that involves the alpha-1 (HBA1) and alpha-2 (HBA2) genes, among others."
    },
    "synonyms": [
        {
            "id": "DOID:0110029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110029",
            "name": "alpha-thalassemia/mental retardation syndrome, type 1",
            "description": ""
        },
        {
            "id": "DOID:0110029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110029",
            "name": "alpha-thalassemia/mental retardation syndrome, deletion-type",
            "description": ""
        },
        {
            "id": "DOID:0110029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110029",
            "name": "ATR syndrome linked to chromosome 16",
            "description": ""
        },
        {
            "id": "DOID:0110029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110029",
            "name": "ATR syndrome, deletion type",
            "description": ""
        },
        {
            "id": "DOID:0110029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110029",
            "name": "ATR-16 syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110029",
            "name": "alpha thalassemia-retardation syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110029",
            "name": "alpha-thalassemia-intellectual disability syndrome linked to chromosome 16",
            "description": ""
        },
        {
            "id": "DOID:0110029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110029",
            "name": "alpha thalassemia-intellectual disability syndrome, deletion type",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "alpha thalassemia-intellectual disability syndrome type 1",
            "description": "Alpha-thalassemia-intellectual deficit syndrome linked to chromosome 16 (ATR-16), a contiguous gene deletion syndrome, is a form of alpha-thalassemia (see this term) characterized by microcytosis, hypochromia, normal hemoglobin (Hb) level or mild anemia, associated with developmental abnormalities."
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "ATR-16 syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "ATR syndrome linked to chromosome 16",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "ALPHA-thalassemia/mental retardation syndrome, chromosome 16-related",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "Alpha thalassemia-mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "alpha-thalassemia-intellectual disability syndrome linked to chromosome 16",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "Alpha-thalassemia/mental retardation syndrome, deletion-type",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "Hemoglobin H-related mental retardation",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "Alpha thalassemia-intellectual disability syndrome, deletion type",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "mental retardation with Hemoglobin H",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "Alpha-thalassemia-intellectual disability syndrome linked to chromosome type 16",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "alpha-thalassemia/mental retardation syndrome, deletion-type",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "alpha thalassemia-retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "ATR, deletion-type",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "ATR syndrome, deletion type",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "chromosome 16P deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "alpha-thalassemia/mental retardation syndrome, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007716",
            "name": "alpha thalassemia-intellectual disability syndrome, deletion type",
            "description": ""
        }
    ]
}