{
    "disease_id": "DOID:0050577", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021093", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021093", 
            "name": "cranioectodermal dysplasia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021093", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021093", 
            "name": "Levin syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021093", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021093", 
            "name": "cranioectodermal dysplasia 1; CED1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021093", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021093", 
            "name": "cranioectodermal dysplasia caused by mutation in IFT122"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021093", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021093", 
            "name": "cranioectodermal dysplasia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021093", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021093", 
            "name": "IFT122 cranioectodermal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021093", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021093", 
            "name": "CED1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021093", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021093", 
            "name": "Sensenbrenner syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050577", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050577", 
            "name": "Sensenbrenner syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050577", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050577", 
            "name": "Levin syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050577", 
        "description": "A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050577", 
        "name": "cranioectodermal dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050577#disease-associations", 
            "id": "0050577", 
            "database": "Alliance of Genome Resources"
        }
    ]
}