{
    "disease_id": "DOID:0110925", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013135", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013135", 
            "name": "HLH5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013135", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013135", 
            "name": "FHL5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013135", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013135", 
            "name": "genetic hemophagocytic lymphohistiocytosis caused by mutation in STXBP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013135", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013135", 
            "name": "HPLH5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013135", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013135", 
            "name": "STXBP2 genetic hemophagocytic lymphohistiocytosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013135", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013135", 
            "name": "hemophagocytic lymphohistiocytosis, familial, 5; FHL5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013135", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013135", 
            "name": "familial hemophagocytic lymphohistiocytosis type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013135", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013135", 
            "name": "hemophagocytic lymphohistiocytosis, familial, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013135", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013135", 
            "name": "hemophagocytic lymphohistiocytosis, familial, type 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110925", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110925", 
            "name": "FHL5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110925", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110925", 
            "name": "HLH5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110925", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110925", 
            "name": "HPLH5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110925", 
        "description": "A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of STXBP2 on chromosome 19p13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110925", 
        "name": "familial hemophagocytic lymphohistiocytosis 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110925#disease-associations", 
            "id": "0110925", 
            "database": "Alliance of Genome Resources"
        }
    ]
}