{
    "disease_id": "DOID:0111705", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010854", 
            "name": "Toriello-Lacassie-Droste syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010854", 
            "name": "oculoectodermal syndrome; oes"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010854", 
            "name": "oculo-ectodermal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010854", 
            "name": "oes"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010854", 
            "name": "aplasia cutis congenita-epibulbar dermoids syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010854", 
            "name": "aplasia cutis congenita with epibulbar dermoids"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010854", 
            "name": "Toriello Lacassie Droste syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111705", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111705", 
            "name": "Toriello-Lacassie-Droste syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111705", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111705", 
            "name": "aplasia cutis congenita-epibulbar dermoids syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111705", 
        "description": "An ectodermal dysplasia characterized by epibulbar dermoids and aplasia cutis congenita that has_material_basis_in somatic mosaic mutation in KRAS on chromosome 12p12.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111705", 
        "name": "oculoectodermal syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111705#disease-associations", 
            "id": "0111705", 
            "database": "Alliance of Genome Resources"
        }
    ]
}