{
    "disease_id": "DOID:0110031",
    "recommended_name": {
        "id": "DOID:0110031",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110031",
        "name": "hemoglobin H disease",
        "description": "An alpha thalassemia that has_material_basis_in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other."
    },
    "synonyms": [
        {
            "id": "DOID:0110031",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110031",
            "name": "HBH",
            "description": ""
        },
        {
            "id": "DOID:0110031",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110031",
            "name": "alpha thalassemia, haemoglobin H type",
            "description": ""
        },
        {
            "id": "DOID:0110031",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110031",
            "name": "alpha thalassemia, hemoglobin H type",
            "description": ""
        },
        {
            "id": "DOID:0110031",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110031",
            "name": "alpha-thalassemia intermedia",
            "description": ""
        },
        {
            "id": "DOID:0110031",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110031",
            "name": "haemoglobin H disease",
            "description": ""
        },
        {
            "id": "DOID:0110031",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110031",
            "name": "haemoglobin H disease, deletional",
            "description": ""
        },
        {
            "id": "DOID:0110031",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110031",
            "name": "hemoglobin H disease, deletional",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "hemoglobin H disease",
            "description": "Alpha thalassemia caused by variation in three of the four copies of the alpha hemoglobin genes (e.g., large deletion in HBA1 and HBA2 genes in trans with a variant in either HBA1 or HBA2)."
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "Alpha-thalassemia intermedia",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "HBA1;HBA2 digenic triallelic hemoglobin H disease",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "HBH",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "HbH",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "HbH disease",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "alpha-thalassemia intermedia",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "haemoglobin H disease, deletional and nondeletional",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "hemoglobin H disease",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "hemoglobin H disease caused by triallelic variation in HBA1;HBA2",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "hemoglobin H disease related to triallelic variation in HBA1 and HBA2",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "hemoglobin H disease, deletional",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "hemoglobin H disease, deletional and nondeletional",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "Alpha-thalassemia, Haemoglobin H type",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "Haemoglobin H disease, Deletional",
            "description": ""
        },
        {
            "id": "MONDO:0013512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013512",
            "name": "Haemoglobin H disease, Nondeletional",
            "description": ""
        },
        {
            "id": "MIM:613978",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613978",
            "name": "Hemoglobin H disease",
            "description": "Hemoglobin H disease"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110031"
    ],
    "unlinked_id_list": []
}