{
    "disease_id": "DOID:0060833", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "Griscelli-Pruniras syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "Griscelli syndrome, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "GS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "Paid syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "hypopigmentation-immunodeficiency with or without neurologic impairment syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "Griscelli syndrome, type 2; GS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "Griscelli disease type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "partial albinism and immunodeficiency syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "Griscelli syndrome with hemophagocytic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011872", 
            "name": "Griscelli-PruniC)ras syndrome type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060833", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060833", 
            "name": "GS2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060833", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060833", 
            "name": "Griscelli syndrome with hemophagocytic syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060833", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060833", 
            "name": "Griscelli-Prunieras syndrome type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060833", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060833", 
            "name": "PAID syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060833", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060833", 
            "name": "partial albinism and immunodeficiency syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060833", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060833", 
            "name": "hypopigmentation-immunodeficiency with or without neurologic impairment syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060833", 
        "description": "A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and immunodeficiency with or without neurologic impairment that has_material_basis_in mutation in the RAB27A gene on chromosome 15q21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060833", 
        "name": "Griscelli syndrome type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060833#disease-associations", 
            "id": "0060833", 
            "database": "Alliance of Genome Resources"
        }
    ]
}