{
    "disease_id": "DOID:0110949", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007862", 
            "name": "Waardenburg syndrome, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007862", 
            "name": "White forelock (poliosis) syndrome with multiple congenital malformations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007862", 
            "name": "WS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007862", 
            "name": "Waardenburg syndrome with limb anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007862", 
            "name": "Waardenburg syndrome type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007862", 
            "name": "Klein-Waardenburg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007862", 
            "name": "Waardenburg syndrome with upper limb anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007862", 
            "name": "Waardenburg syndrome, type 3; WS3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110949", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110949", 
            "name": "Klein-Waardenburg syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110949", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110949", 
            "name": "WS3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110949", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110949", 
            "name": "Waardenburg syndrome type III"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110949", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110949", 
            "name": "Waardenburg syndrome with upper limb anomalies"
        }, 
        {
            "url": "https://www.omim.org/entry/148820", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:148820", 
            "name": "Waardenburg syndrome 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110949", 
        "description": "A Waardenburg's syndrome characterized by upper limb anomalies, congenital hearing loss, dystopia canthorum and pigmentation anomalies of eyes, hair, and skin that has_material_basis_in heterozygous or homozygous mutation in the PAX3 gene on chromosome 2q36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110949", 
        "name": "Waardenburg syndrome type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/148820", 
            "id": "148820", 
            "database": "MIM"
        }
    ]
}