{
    "disease_id": "DOID:0110950", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008671", 
            "name": "Waardenburg syndrome, type 2A; WS2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008671", 
            "name": "Waardenburg syndrome type IIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008671", 
            "name": "WS2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008671", 
            "name": "Ws2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008671", 
            "name": "Waardenburg syndrome type 2 caused by mutation in MITF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008671", 
            "name": "Waardenburg syndrome, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008671", 
            "name": "MITF Waardenburg syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008671", 
            "name": "Waardenburg syndrome without dystopia canthorum"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110950", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110950", 
            "name": "WS2A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110950", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110950", 
            "name": "Waardenburg syndrome type IIA"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110950", 
        "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 heterozygous mutation in the MITF gene on chromosome 3p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110950", 
        "name": "Waardenburg syndrome type 2A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110950#disease-associations", 
            "id": "0110950", 
            "database": "Alliance of Genome Resources"
        }
    ]
}