{
    "disease_id": "DOID:0110917", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000913", 
            "name": "spherocytosis, hereditary, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000913", 
            "name": "spherocytosis, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000913", 
            "name": "SPTB hereditary spherocytosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000913", 
            "name": "HS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000913", 
            "name": "hereditary spherocytosis 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000913", 
            "name": "spherocytosis, type 2; SPH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000913", 
            "name": "SPH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000913", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000913", 
            "name": "hereditary spherocytosis caused by mutation in SPTB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110917", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110917", 
            "name": "HS2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110917", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110917", 
            "name": "SPH2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110917", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110917", 
            "name": "hereditary spherocytosis 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110917", 
        "description": "A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of SPTB on chromosome 14q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110917", 
        "name": "hereditary spherocytosis type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110917#disease-associations", 
            "id": "0110917", 
            "database": "Alliance of Genome Resources"
        }
    ]
}