{
    "disease_id": "DOID:0070022",
    "recommended_name": {
        "id": "DOID:0070022",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070022",
        "name": "autosomal recessive dyskeratosis congenita 5",
        "description": "A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the RTEL1 gene on chromosome 20q13.33."
    },
    "synonyms": [
        {
            "id": "DOID:0070022",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070022",
            "name": "DKCB5",
            "description": ""
        },
        {
            "id": "MONDO:0014076",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014076",
            "name": "dyskeratosis congenita, autosomal recessive 5",
            "description": "A dyskeratosis congenita that has material basis in an autosomal dominant mutation of RTEL1 on chromosome 20q13.33."
        },
        {
            "id": "MONDO:0014076",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014076",
            "name": "DKCB5",
            "description": ""
        },
        {
            "id": "MONDO:0014076",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014076",
            "name": "dyskeratosis congenita, autosomal recessive 5",
            "description": ""
        },
        {
            "id": "MONDO:0014076",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014076",
            "name": "dyskeratosis congenita, autosomal recessive type 5",
            "description": ""
        },
        {
            "id": "MIM:615190",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615190",
            "name": "Dyskeratosis congenita, autosomal recessive, 5",
            "description": "Dyskeratosis congenita, autosomal recessive, 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070022"
    ],
    "unlinked_id_list": []
}