{
    "disease_id": "DOID:0110918", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010053", 
            "name": "spherocytosis, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010053", 
            "name": "HS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010053", 
            "name": "hereditary spherocytosis caused by mutation in SPTA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010053", 
            "name": "spherocytosis, hereditary, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010053", 
            "name": "hereditary spherocytosis 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010053", 
            "name": "SPH3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010053", 
            "name": "SPTA1 hereditary spherocytosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010053", 
            "name": "spherocytosis, type 3; SPH3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110918", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110918", 
            "name": "HS3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110918", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110918", 
            "name": "SPH3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110918", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110918", 
            "name": "hereditary spherocytosis 3"
        }, 
        {
            "url": "https://www.omim.org/entry/270970", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:270970", 
            "name": "Spherocytosis 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110918", 
        "description": "A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110918", 
        "name": "hereditary spherocytosis type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/270970", 
            "id": "270970", 
            "database": "MIM"
        }
    ]
}