{
    "disease_id": "DOID:0070024", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014600", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014600", 
            "name": "dyskeratosis congenita, autosomal recessive 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014600", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014600", 
            "name": "dyskeratosis congenita, autosomal recessive 6; DKCB6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014600", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014600", 
            "name": "DKCB6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014600", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014600", 
            "name": "dyskeratosis congenita caused by mutation in PARN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014600", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014600", 
            "name": "PARN dyskeratosis congenita"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014600", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014600", 
            "name": "dyskeratosis congenita, autosomal recessive type 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070024", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070024", 
            "name": "DKCB6"
        }, 
        {
            "url": "https://www.omim.org/entry/616353", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616353", 
            "name": "Dyskeratosis congenita, autosomal recessive, 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070024", 
        "description": "A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of PARN on chromosome 16p13.12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070024", 
        "name": "autosomal recessive dyskeratosis congenita 6"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616353", 
            "id": "616353", 
            "database": "MIM"
        }
    ]
}