{
    "disease_id": "DOID:0070026", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009990", 
            "name": "dyskeratosis congenita with bilateral exudative retinopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009990", 
            "name": "dyskeratosis congenita, autosomal dominant 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009990", 
            "name": "retinopathy-anemia-central nervous system anomalies syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009990", 
            "name": "DKCA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009990", 
            "name": "exudative retinopathy with bone marrow failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009990", 
            "name": "Revesz-DeBuse syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070026", 
            "name": "DKCA5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070026", 
            "name": "Dyskeratosis Congenita, Autosomal Dominant 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070026", 
            "name": "exudative retinopathy with bone marrow failure"
        }, 
        {
            "url": "https://www.omim.org/entry/268130", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:268130", 
            "name": "Dyskeratosis congenita, autosomal dominant, 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070026", 
        "description": "A dyskeratosis congenita that has_material_basis_in a mutation of TINF2 on chromosome 14q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070026", 
        "name": "Revesz syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/268130", 
            "id": "268130", 
            "database": "MIM"
        }
    ]
}