{
    "disease_id": "DOID:0110951",
    "recommended_name": {
        "id": "DOID:0110951",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110951",
        "name": "Waardenburg syndrome type 2C",
        "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 variation in the chromosome region 8p23."
    },
    "synonyms": [
        {
            "id": "DOID:0110951",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110951",
            "name": "WS2C",
            "description": ""
        },
        {
            "id": "DOID:0110951",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110951",
            "name": "Waardenburg syndrome type IIC",
            "description": ""
        },
        {
            "id": "MONDO:0011697",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011697",
            "name": "Waardenburg syndrome type 2C",
            "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 variation in the chromosome region 8p23."
        },
        {
            "id": "MONDO:0011697",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011697",
            "name": "WS2C",
            "description": ""
        },
        {
            "id": "MONDO:0011697",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011697",
            "name": "Waardenburg syndrome type IIC",
            "description": ""
        },
        {
            "id": "MONDO:0011697",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011697",
            "name": "Waardenburg syndrome, type 2C",
            "description": ""
        },
        {
            "id": "MONDO:0011697",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011697",
            "name": "Waardenburg syndrome, type 2C; WS2C",
            "description": ""
        }
    ]
}