{
    "disease_id": "DOID:0110916",
    "recommended_name": {
        "id": "DOID:0110916",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110916",
        "name": "hereditary spherocytosis type 1",
        "description": "A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of ANK1 on chromosome 8p11.21."
    },
    "synonyms": [
        {
            "id": "DOID:0110916",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110916",
            "name": "HS1",
            "description": ""
        },
        {
            "id": "DOID:0110916",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110916",
            "name": "SPH1",
            "description": ""
        },
        {
            "id": "DOID:0110916",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110916",
            "name": "hereditary spherocytosis 1",
            "description": ""
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "hereditary spherocytosis type 1",
            "description": "Any hereditary spherocytosis in which the cause of the disease is a mutation in the ANK1 gene."
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "hereditary spherocytosis 1",
            "description": ""
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "spherocytosis, type 1; SPH1",
            "description": ""
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "spherocytosis, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "spherocytosis, hereditary, 1",
            "description": ""
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "Sph",
            "description": ""
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "SPH1",
            "description": ""
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "HS1",
            "description": ""
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "hereditary spherocytosis caused by mutation in ANK1",
            "description": ""
        },
        {
            "id": "MONDO:0008447",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008447",
            "name": "ANK1 hereditary spherocytosis",
            "description": ""
        },
        {
            "id": "MIM:182900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/182900",
            "name": "Spherocytosis 1",
            "description": "Spherocytosis 1"
        }
    ]
}
