{
    "disease_id": "DOID:0110953", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "Waardenburg syndrome type IVA"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "EDNRB Waardenburg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "Waardenburg-Shah syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "Shah-Waardenburg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "Ws4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "Waardenburg syndrome, type 4A; WS4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "Waardenburg syndrome with Hirschsprung disease type 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "Waardenburg syndrome caused by mutation in EDNRB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "Waardenburg syndrome with Hirschsprung disease, type 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "Waardenburg syndrome, type 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010192", 
            "name": "WS4A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110953", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110953", 
            "name": "WS4A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110953", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110953", 
            "name": "Waardenburg syndrome type IVA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110953", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110953", 
            "name": "Waardenburg syndrome with Hirschsprung disease type 4A"
        }, 
        {
            "url": "https://www.omim.org/entry/277580", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:277580", 
            "name": "Waardenburg syndrome 4A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110953", 
        "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 heterozygous or homozygous mutation in the EDNRB gene on chromosome 13q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110953", 
        "name": "Waardenburg syndrome type 4A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/277580", 
            "id": "277580", 
            "database": "MIM"
        }
    ]
}