{
    "disease_id": "DOID:0110031", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013512", 
            "name": "Hemoglobin H disease, Deletional"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013512", 
            "name": "HbH disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013512", 
            "name": "alpha-thalassemia intermedia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013512", 
            "name": "HEMOGLOBIN H disease; HbH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013512", 
            "name": "alpha thalassemia, hemoglobin H type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013512", 
            "name": "Hemoglobin H disease, Nondeletional"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013512", 
            "name": "HbH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013512", 
            "name": "Alpha-thalassemia, Hemoglobin H type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110031", 
            "name": "HBH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110031", 
            "name": "alpha thalassemia, haemoglobin H type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110031", 
            "name": "alpha thalassemia, hemoglobin H type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110031", 
            "name": "alpha-thalassemia intermedia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110031", 
            "name": "haemoglobin H disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110031", 
            "name": "haemoglobin H disease, deletional"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110031", 
            "name": "hemoglobin H disease, deletional"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110031", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110031", 
        "name": "hemoglobin H disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613978", 
            "id": "613978", 
            "database": "MIM"
        }
    ]
}