{
    "disease_id": "DOID:0110952", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012144", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012144", 
            "name": "SNAI2 Waardenburg syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012144", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012144", 
            "name": "Waardenburg syndrome type 2 caused by mutation in SNAI2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012144", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012144", 
            "name": "WS2D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012144", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012144", 
            "name": "Waardenburg syndrome, type 2D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012144", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012144", 
            "name": "Waardenburg syndrome type IID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012144", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012144", 
            "name": "Waardenburg syndrome, type 2D; WS2D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110952", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110952", 
            "name": "WS2D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110952", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110952", 
            "name": "Waardenburg syndrome type IID"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110952", 
        "description": "A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in homozygous deletion of the SNAI2 gene on chromosome 8q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110952", 
        "name": "Waardenburg syndrome type 2D"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110952#disease-associations", 
            "id": "0110952", 
            "database": "Alliance of Genome Resources"
        }
    ]
}