{
    "disease_id": "DOID:2373",
    "recommended_name": {
        "id": "DOID:2373",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2373",
        "name": "hereditary elliptocytosis",
        "description": "A hematopoietic system disease characterized by oval or elliptical red blood cells, slight or absent hemolysis with little or no anemia; splenomegaly is often present."
    },
    "synonyms": [
        {
            "id": "DOID:2373",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2373",
            "name": "Congenital elliptocytosis",
            "description": ""
        },
        {
            "id": "DOID:2373",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2373",
            "name": "ovalocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0007533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007533",
            "name": "elliptocytosis 2",
            "description": "Any hereditary elliptocytosis in which the cause of the disease is a mutation in the SPTA1 gene."
        },
        {
            "id": "MONDO:0007533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007533",
            "name": "elliptocytosis 2",
            "description": ""
        },
        {
            "id": "MONDO:0007533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007533",
            "name": "elliptocytosis, Rhesus-unlinked type",
            "description": ""
        },
        {
            "id": "MONDO:0007533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007533",
            "name": "EL2",
            "description": ""
        },
        {
            "id": "MONDO:0007533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007533",
            "name": "SPTA1 hereditary elliptocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0007533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007533",
            "name": "elliptocytosis type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007533",
            "name": "elliptocytosis 2; EL2",
            "description": ""
        },
        {
            "id": "MONDO:0007533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007533",
            "name": "hereditary elliptocytosis caused by mutation in SPTA1",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "elliptocytosis 1",
            "description": "Any hereditary elliptocytosis in which the cause of the disease is a mutation in the EPB41 gene."
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "Protein 4.1 of erythrocyte Membrane, defect of",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "elliptocytosis 1; EL1",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "elliptocytosis, Rhesus-linked type",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "elliptocytosis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "EPB41 hereditary elliptocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "hereditary elliptocytosis caused by mutation in EPB41",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "4.1-minus trait",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "elliptocytosis 1",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "4.1- trait",
            "description": ""
        },
        {
            "id": "MONDO:0012731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012731",
            "name": "EL1",
            "description": ""
        },
        {
            "id": "MIM:130600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/130600",
            "name": "Elliptocytosis 2",
            "description": "Elliptocytosis 2"
        },
        {
            "id": "MIM:611804",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611804",
            "name": "Elliptocytosis 1",
            "description": "Elliptocytosis 1"
        }
    ]
}