{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007533", 
            "name": "elliptocytosis 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007533", 
            "name": "elliptocytosis, Rhesus-unlinked type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007533", 
            "name": "EL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007533", 
            "name": "SPTA1 hereditary elliptocytosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007533", 
            "name": "elliptocytosis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007533", 
            "name": "elliptocytosis 2; EL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007533", 
            "name": "hereditary elliptocytosis caused by mutation in SPTA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2373", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2373", 
            "name": "Congenital elliptocytosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2373", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2373", 
            "name": "ovalocytosis"
        }, 
        {
            "url": "https://www.omim.org/entry/130600", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:130600", 
            "name": "Elliptocytosis 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2373", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2373", 
        "name": "hereditary elliptocytosis"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/130600", 
            "id": "130600", 
            "database": "MIM"
        }
    ]
}