{
    "disease_id": "DOID:0050780", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "X-linked Opitz G/BBB syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "Opitz GBBB syndrome, type I; GBBB1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "Opitz GBBB syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "Opitz GBBB syndrome, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "XLOS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "Opitz syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "hypertelorism with esophageal Abnormality and hypospadias"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "Opitz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "Opitz GBBB syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "hypertelorism-hypospadias syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "X-linked Opitz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "GBBB1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "Opitz G/BBB syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "telecanthus-hypospadias syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "Opitz Bbbg syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "Opitz-G syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010222", 
            "name": "X-linked Opitz BBB/G syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050780", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050780", 
            "name": "Opitz G/BBB Syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/300000", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300000", 
            "name": "Opitz GBBB syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050780", 
        "description": "A syndrome that is characterized by hypertelorism, hypospadias, and additional midline defects.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050780", 
        "name": "Opitz-GBBB syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300000", 
            "id": "300000", 
            "database": "MIM"
        }
    ]
}