{
    "disease_id": "DOID:0080631", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008885", 
            "name": "Branchioskeletogenital syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008885", 
            "name": "branchio-skeleto-genital syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008885", 
            "name": "BRACHIOSKELETOGENITAL syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008885", 
            "name": "ELSAHY-Waters syndrome; ESWS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008885", 
            "name": "ESWS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008885", 
            "name": "BSG syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080631", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080631", 
            "name": "branchioskeletogenital syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080631", 
        "description": "A syndrome that is characterized by brachycephaly, facial asymmetry, marked hypertelorism, proptosis, blepharochalasis, midface hypoplasia, broad nose with concave nasal ridge, and prognathism; radicular dentin dysplasia with consequent obliterated pulp chambers, apical translucent cysts, recurrent infections, and early loss of teeth; vertebral fusions, particularly at C2-C3; and moderate mental retardation.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080631", 
        "name": "Elsahy-Waters syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080631#disease-associations", 
            "id": "0080631", 
            "database": "Alliance of Genome Resources"
        }
    ]
}