{
    "disease_id": "DOID:0081332",
    "recommended_name": {
        "id": "DOID:0081332",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081332",
        "name": "progeroid syndrome",
        "description": "A syndrome that is characterized by the premature onset of age-related pathologies."
    },
    "synonyms": [
        {
            "id": "DOID:0081332",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081332",
            "name": "progeroid disease",
            "description": ""
        },
        {
            "id": "DOID:0081332",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081332",
            "name": "progeroid syndromes",
            "description": ""
        },
        {
            "id": "MONDO:0008310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008310",
            "name": "Hutchinson-Gilford progeria syndrome",
            "description": "Hutchinson-Gilford progeria syndrome is a rare, fatal, autosomal dominant and premature aging disease, beginning in childhood and characterized by growth reduction, failure to thrive, a typical facial appearance (prominent forehead, protuberant eyes, thin nose with a beaked tip, thin lips, micrognathia and protruding ears) and distinct dermatologic features (generalized alopecia, aged-looking skin, sclerotic and dimpled skin over the abdomen and extremities, prominent cutaneous vasculature, dyspigmentation, nail hypoplasia and loss of subcutaneous fat)."
        },
        {
            "id": "MONDO:0008310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008310",
            "name": "progeria",
            "description": ""
        },
        {
            "id": "MONDO:0008310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008310",
            "name": "HGPS",
            "description": ""
        },
        {
            "id": "MONDO:0008310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008310",
            "name": "Hutchinson-Gilford disease",
            "description": ""
        },
        {
            "id": "MONDO:0008310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008310",
            "name": "Hutchinson-Gilford progeria",
            "description": ""
        },
        {
            "id": "MONDO:0008310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008310",
            "name": "Hutchinson-Gilford progeria syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008310",
            "name": "premature senility syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008310",
            "name": "Hutchinson Gilford progeria syndrome",
            "description": ""
        },
        {
            "id": "MIM:176670",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/176670",
            "name": "Hutchinson-Gilford progeria syndrome",
            "description": "Hutchinson-Gilford progeria syndrome"
        }
    ],
    "children": [
        {
            "id": "DOID:0051067",
            "label": "Fontaine progeroid syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060590",
            "label": "XFE progeroid syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0081333",
            "label": "Wiedemann-Rautenstrauch syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0081334",
            "label": "Nestor-Guillermo progeria syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:3911",
            "label": "progeria",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:5688",
            "label": "Werner syndrome",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0060590",
        "DOID:0081333",
        "DOID:5688",
        "DOID:3911",
        "DOID:0051067",
        "DOID:0081332",
        "DOID:0081334"
    ],
    "unlinked_id_list": []
}