{
    "disease_id": "DOID:0050471", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "Carney complex, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "PRKAR1A Carney complex"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "Carney complex caused by mutation in PRKAR1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "CARNEY complex, type 1; CNC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "Myxoma, spotty pigmentation, and endocrine overactivity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "Carney Myxoma-endocrine Complex"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "lamb syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "name syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "Carney syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008057", 
            "name": "CNC1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050471", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050471", 
            "name": "Carney Complex, Type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050471", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050471", 
            "name": "Carney Complex, Type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050471", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050471", 
            "name": "Carney Syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050471", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050471", 
            "name": "Carney complex variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050471", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050471", 
            "name": "LAMB Syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050471", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050471", 
            "name": "NAME Syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050471", 
        "description": "A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050471", 
        "name": "Carney complex"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050471#disease-associations", 
            "id": "0050471", 
            "database": "Alliance of Genome Resources"
        }
    ]
}