{
    "disease_id": "DOID:0110948", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008670", 
            "name": "Waardenburg syndrome, type 1; WS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008670", 
            "name": "Waardenburg's syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008670", 
            "name": "Waardenburg syndrome type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008670", 
            "name": "WS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008670", 
            "name": "Waardenburg syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008670", 
            "name": "Waardenburg syndrome with dystopia canthorum"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110948", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110948", 
            "name": "WS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110948", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110948", 
            "name": "Waardenburg syndrome type I"
        }, 
        {
            "url": "https://www.omim.org/entry/193500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:193500", 
            "name": "Waardenburg syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110948", 
        "description": "A Waardenburg's syndrome characterized by autosomal dominant inheritance of congenital deafness, pigmentation anomalies of eyes, hair, and skin,and dystopia canthorum that has_material_basis_in heterozygous mutation in the PAX3 gene on chromosome 2q36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110948", 
        "name": "Waardenburg syndrome type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/193500", 
            "id": "193500", 
            "database": "MIM"
        }
    ]
}