{
    "disease_id": "DOID:3263", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008244", 
            "name": "partial albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008244", 
            "name": "piebald trait"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008244", 
            "name": "piebald trait; PBT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008244", 
            "name": "PBT"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3263", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3263", 
            "name": "PIEBALD TRAIT"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3263", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3263", 
            "name": "Partial albinism"
        }, 
        {
            "url": "https://www.omim.org/entry/172800", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:172800", 
            "name": "Piebald trait"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3263", 
        "description": "An integumentary system disease characterized by congenital absence of melanocytes in areas of the skin and hair that has_material_basis_in heterozygous mutation in either KIT or SNAI2 on chromosome 4q12 or 8q11.21, respectively.", 
        "resource": "Disease Ontology", 
        "id": "DOID:3263", 
        "name": "piebaldism"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/172800", 
            "id": "172800", 
            "database": "MIM"
        }
    ]
}