{
    "disease_id": "DOID:0080345", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "BCD syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "Lagophthalmia with bilateral cleft 51P and palate"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "blepharocheilodontic syndrome 1; BCDS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "CDH1 blepharo-cheilo-odontic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "blepharo-cheilo-odontic syndrome caused by mutation in CDH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "elschnig syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "clefting, ectropion, and conical teeth"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "BCDS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "ectropion, Inferior, with cleft 51P and/Or palate"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054740", 
            "name": "blepharocheilodontic syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080345", 
        "description": "A blepharocheilodontic syndrome that has_material_basis_in heterozygous mutation in the CDH1 gene on chromosome 16q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080345", 
        "name": "blepharocheilodontic syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080345#disease-associations", 
            "id": "0080345", 
            "database": "Alliance of Genome Resources"
        }
    ]
}
