{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011269", 
            "name": "CARD14 psoriasis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011269", 
            "name": "psoriasis caused by mutation in CARD14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011269", 
            "name": "psoriasis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011269", 
            "name": "PSORS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011269", 
            "name": "psoriasis 2; PSORS2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080475", 
        "description": "A psoriasis that has_material_basis_in heterozygous mutation in the CARD14 gene on chromosome 17q25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080475", 
        "name": "psoriasis 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/602723", 
            "id": "602723", 
            "database": "MIM"
        }
    ]
}