{
    "disease_id": "DOID:0060541", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013555", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013555", 
            "name": "Hermansky-Pudlak syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013555", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013555", 
            "name": "Hermansky-Pudlak syndrome caused by mutation in HPS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013555", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013555", 
            "name": "HPS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013555", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013555", 
            "name": "HPS3 Hermansky-Pudlak syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013555", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013555", 
            "name": "Hermansky-Pudlak syndrome 3; HPS3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060541", 
        "description": "A Hermasky-Pudlak syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the HPS3 gene on chromosome 3q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060541", 
        "name": "Hermansky-Pudlak syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614072", 
            "id": "614072", 
            "database": "MIM"
        }
    ]
}