{
    "disease_id": "DOID:0060856", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "right atrial isomerism (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "asplenia with cardiovascular anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "Polyasplenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "right isomerism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "Ivemark syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "heterotaxy, Visceroatrial, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "RAI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "asplenia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "bilateral right-sidedness sequence"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "Vah, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "right atrial isomerism; RAI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "polysplenia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008832", 
            "name": "splenic agenesis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060856", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060856", 
            "name": "Ivemark syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060856", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060856", 
            "name": "asplenia with cardiovascular anomalies"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060856", 
        "description": "A visceral heterotaxy that is characterized by complete atrioventricular septal defect with a common atrium and univentricular AV connection, total anomalous pulmonary drainage, and transposition or malposition of the great arteries and that has_material_basis_in homozygous mutation in the GDF1 gene on chromosome 19p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060856", 
        "name": "right atrial isomerism"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060856#disease-associations", 
            "id": "0060856", 
            "database": "Alliance of Genome Resources"
        }
    ]
}