{
    "disease_id": "DOID:0060834", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012220", 
            "name": "Griscelli-PruniC)ras syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012220", 
            "name": "Griscelli syndrome, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012220", 
            "name": "GS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012220", 
            "name": "Griscelli-Pruniras syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012220", 
            "name": "Griscelli syndrome, type 3; GS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012220", 
            "name": "Griscelli disease type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012220", 
            "name": "hypomelanosis with no immunologic or neurologic manifestations"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060834", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060834", 
            "name": "GS3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060834", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060834", 
            "name": "Griscelli-Prunieras syndrome type 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060834", 
        "description": "A Griscelli syndrome characterized by isolated silvery gray sheen of the hair and hypopigmentation of the skin that has_material_basis_in mutation in the MLPH or MYO5A genes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060834", 
        "name": "Griscelli syndrome type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060834#disease-associations", 
            "id": "0060834", 
            "database": "Alliance of Genome Resources"
        }
    ]
}