{
    "disease_id": "DOID:0110920", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012985", 
            "name": "hereditary spherocytosis 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012985", 
            "name": "spherocytosis, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012985", 
            "name": "spherocytosis, hereditary, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012985", 
            "name": "hereditary spherocytosis caused by mutation in EPB42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012985", 
            "name": "HS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012985", 
            "name": "spherocytosis, type 5; SPH5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012985", 
            "name": "EPB42 hereditary spherocytosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012985", 
            "name": "SPH5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110920", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110920", 
            "name": "HS5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110920", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110920", 
            "name": "SPH5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110920", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110920", 
            "name": "hereditary spherocytosis 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110920", 
        "description": "A hereditary spherocytosis that has_material_basis_in a mutation of EPB42 on chromosome 15q15.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110920", 
        "name": "hereditary spherocytosis type 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110920#disease-associations", 
            "id": "0110920", 
            "database": "Alliance of Genome Resources"
        }
    ]
}