{
    "disease_id": "DOID:0050462", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020667", 
            "name": "Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020667", 
            "name": "ABS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020667", 
            "name": "trapezoidocephaly-synostosis Syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020667", 
            "name": "multisynostotic osteodysgenesis with long bone fractures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020667", 
            "name": "Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis; ABS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020667", 
            "name": "osteodysgenesis, multisynostotic, with fractures"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050462", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050462", 
            "name": "trapezoidocephaly-synostosis syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050462", 
        "description": "A syndrome that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050462", 
        "name": "Antley-Bixler syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050462#disease-associations", 
            "id": "0050462", 
            "database": "Alliance of Genome Resources"
        }
    ]
}