{
    "disease_id": "DOID:0060834",
    "recommended_name": {
        "id": "DOID:0060834",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060834",
        "name": "Griscelli syndrome type 3",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060834",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060834",
            "name": "GS3",
            "description": ""
        },
        {
            "id": "DOID:0060834",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060834",
            "name": "Griscelli-Prunieras syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012220",
            "name": "Griscelli syndrome type 3",
            "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."
        },
        {
            "id": "MONDO:0012220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012220",
            "name": "GS3",
            "description": ""
        },
        {
            "id": "MONDO:0012220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012220",
            "name": "Griscelli syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012220",
            "name": "Griscelli-PruniC)ras syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012220",
            "name": "Griscelli-Pruniras syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012220",
            "name": "Griscelli syndrome, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012220",
            "name": "hypomelanosis with no immunologic or neurologic manifestations",
            "description": ""
        },
        {
            "id": "MIM:609227",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609227",
            "name": "Griscelli syndrome 3",
            "description": "Griscelli syndrome 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060834"
    ],
    "unlinked_id_list": []
}