{
    "disease_id": "DOID:0080663", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014329", 
            "name": "atrial standstill type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014329", 
            "name": "atrial standstill caused by mutation in NPPA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014329", 
            "name": "atrial standstill 2; ATRST2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014329", 
            "name": "NPPA atrial standstill"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014329", 
            "name": "atrial dilation and standstill"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014329", 
            "name": "cardiomyopathy, atrial dilated, with atrial standstill"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014329", 
            "name": "ATRST2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080663", 
        "description": "A heart conduction disease that is characterized by a transient or permanent absence of electrical and mechanical atrial activity and has_material_basis_in homozygous mutation in the NPPA gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080663", 
        "name": "atrial standstill 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615745", 
            "id": "615745", 
            "database": "MIM"
        }
    ]
}