{
    "disease_id": "DOID:0111591", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009008", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009008", 
            "name": "heart defect - tongue hamartoma - polysyndactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009008", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009008", 
            "name": "Ostravik-Lindemann-Solberg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009008", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009008", 
            "name": "CHDTHP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009008", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009008", 
            "name": "congenital heart defects, hamartomas of tongue, and polysyndactyly; CHDTHP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009008", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009008", 
            "name": "Orstavik Lindemann Solberg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009008", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009008", 
            "name": "heart defect, tongue hamartoma and polysyndactyly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111591", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111591", 
            "name": "CHDTHP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111591", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111591", 
            "name": "Ostravik-Lindemann-Solberg syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111591", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111591", 
            "name": "heart defect-tongue hamartoma-polysyndactyly syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111591", 
        "description": "A syndrome characterized by congenital heart defects, hamartomas of tongue, and polysyndactyly that has_material_basis_in homozygous or compound heterozygous mutation in WDPCP on chromosome 2p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111591", 
        "name": "congenital heart defects, hamartomas of tongue, and polysyndactyly"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111591#disease-associations", 
            "id": "0111591", 
            "database": "Alliance of Genome Resources"
        }
    ]
}