{
    "disease_id": "DOID:0110954", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013201", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013201", 
            "name": "Waardenburg syndrome, type 4B; WS4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013201", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013201", 
            "name": "Waardenburg syndrome, type 4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013201", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013201", 
            "name": "Waardenburg syndrome with Hirschsprung disease type 4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013201", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013201", 
            "name": "EDN3 Waardenburg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013201", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013201", 
            "name": "WS4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013201", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013201", 
            "name": "Waardenburg syndrome type IVB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013201", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013201", 
            "name": "Waardenburg syndrome, type 4B, with Hirschsprung disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013201", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013201", 
            "name": "Waardenburg syndrome caused by mutation in EDN3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110954", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110954", 
            "name": "WS4B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110954", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110954", 
            "name": "Waardenburg syndrome type IVB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110954", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110954", 
            "name": "Waardenburg syndrome with Hirschsprung disease type 4B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110954", 
        "description": "A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and Hirschsprung disease that has_material_basis_in homozygous and heterozygous mutation in the EDN3 gene on chromosome 20q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110954", 
        "name": "Waardenburg syndrome type 4B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110954#disease-associations", 
            "id": "0110954", 
            "database": "Alliance of Genome Resources"
        }
    ]
}