{
    "disease_id": "DOID:11725", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "Cornelia de Lange syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "Cdl"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "De Lange syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "Brachmann-De Lange syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "CDLS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "NIPBL Cornelia de Lange syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "Cornelia De Lange syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "Cornelia DE Lange syndrome 1; CDLS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "typus Degenerativus Amstelodamensis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007387", 
            "name": "Cornelia de Lange syndrome caused by mutation in NIPBL"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11725", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11725", 
            "name": "Brachmann de Lange syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11725", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11725", 
            "name": "De Lange syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:11725", 
        "description": "A syndrome that is characterized by slow growth before and after birth, intellectual disability that is usually severe to profound, skeletal abnormalities involving the arms and hands, and distinctive facial features.", 
        "resource": "Disease Ontology", 
        "id": "DOID:11725", 
        "name": "Cornelia de Lange syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/11725#disease-associations", 
            "id": "11725", 
            "database": "Alliance of Genome Resources"
        }
    ]
}