{
    "disease_id": "DOID:0081333",
    "recommended_name": {
        "id": "DOID:0081333",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081333",
        "name": "Wiedemann-Rautenstrauch syndrome",
        "description": "A progeroid syndrome that is characterized by intrauterine growth retardation, failure to thrive, short stature, a progeroid appearance, hypotonia, and variable mental impairment and that has_material_basis_in compound heterozygous mutation in the POLR3A gene on chromosome 10q22."
    },
    "synonyms": [
        {
            "id": "DOID:0081333",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081333",
            "name": "Neonatal progeroid syndrome",
            "description": ""
        },
        {
            "id": "DOID:0081333",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081333",
            "name": "PROGEROID SYNDROME, NEONATAL",
            "description": ""
        },
        {
            "id": "MONDO:0009910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009910",
            "name": "Wiedemann-Rautenstrauch syndrome",
            "description": "Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism."
        },
        {
            "id": "MONDO:0009910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009910",
            "name": "Wiedemann Rautenstrauch Syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009910",
            "name": "Wiedemann-Rautenstrauch syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009910",
            "name": "neonatal progeroid syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009910",
            "name": "Wiedemann Rautenstrauch syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009910",
            "name": "progeroid syndrome neonatal",
            "description": ""
        },
        {
            "id": "MIM:264090",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/264090",
            "name": "Wiedemann-Rautenstrauch syndrome",
            "description": "Wiedemann-Rautenstrauch syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081333"
    ],
    "unlinked_id_list": []
}