{
    "disease_id": "DOID:0060831", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli-PruniC)ras syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "GS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "hypopigmentation-neurologic impairment syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "pigmentary dilution of the skin and hair, the presence of large clumps of pigment in hair shafts"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli-Pruniras syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli syndrome, cutaneous and neurological type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli syndrome with neurological impairment"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "partial albinism and primary neurologic disease without hemophagocytic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli syndrome, cutaneous and neurologic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli syndrome, type 1; GS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli disease type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008962", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008962", 
            "name": "Griscelli syndrome with neurologic impairment"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060831", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060831", 
            "name": "Chediak-Higashi-like syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060831", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060831", 
            "name": "Griscelli-Prunieras syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060831", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060831", 
            "name": "partial albinism-immunodeficiency syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/214450", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:214450", 
            "name": "Griscelli syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060831", 
        "description": "An integumentary system disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060831", 
        "name": "Griscelli syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/214450", 
            "id": "214450", 
            "database": "MIM"
        }
    ]
}