{
    "disease_id": "DOID:0070114", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011873", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011873", 
            "name": "Niemann-Pick disease, type C2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011873", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011873", 
            "name": "Niemann-PICK disease, type C2; NPC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011873", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011873", 
            "name": "NPC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011873", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011873", 
            "name": "type C2 Niemann-Pick disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070114", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070114", 
            "name": "NPC2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070114", 
        "description": "A Niemann-Pick disease that has_material_basis_in an autosomal recessive mutation of NPC2 on chromosome 14q24.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070114", 
        "name": "Niemann-Pick disease type C2"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011873", 
            "id": "0011873", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/607625", 
            "id": "607625", 
            "database": "MIM"
        }
    ]
}