{
    "disease_id": "DOID:0060831",
    "recommended_name": {
        "id": "DOID:0060831",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060831",
        "name": "Griscelli syndrome",
        "description": "An integumentary system disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin."
    },
    "synonyms": [
        {
            "id": "DOID:0060831",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060831",
            "name": "Chediak-Higashi-like syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060831",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060831",
            "name": "Griscelli-Prunieras syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060831",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060831",
            "name": "partial albinism-immunodeficiency syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008962",
            "name": "Griscelli syndrome type 1",
            "description": "A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and neurological impairment without immunodeficiency that has material basis in mutations in the MYO5A gene on chromosome 15q21.2."
        },
        {
            "id": "MONDO:0008962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008962",
            "name": "GS1",
            "description": ""
        },
        {
            "id": "MONDO:0008962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008962",
            "name": "Griscelli syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008962",
            "name": "Griscelli-PruniC)ras syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008962",
            "name": "Griscelli-Pruniras syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008962",
            "name": "hypopigmentation-neurologic impairment syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008962",
            "name": "Griscelli syndrome, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008962",
            "name": "pigmentary dilution of the skin and hair, the presence of large clumps of pigment in hair shafts",
            "description": ""
        },
        {
            "id": "MIM:214450",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/214450",
            "name": "Griscelli syndrome 1",
            "description": "Griscelli syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0060832",
            "label": "Griscelli syndrome type 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060833",
            "label": "Griscelli syndrome type 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060834",
            "label": "Griscelli syndrome type 3",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0060831",
        "DOID:0060832",
        "DOID:0060834",
        "DOID:0060833"
    ],
    "unlinked_id_list": []
}